68 jobs in IQVIA

**Job Overview**
Support the growth of the Medical Affairs business by providing business development, lead generation, opportunity management, and sales operations support. Working closely with Medical Affairs, Business Development, and Commercial teams, this role is responsible for identifying and qualifying new business opportunities, maintaining sales pipeline visibility, coordinating proposal development activities, and ensuring accurate CRM and forecasting management. The role contributes to business growth by enabling efficient customer engagement, supporting strategic sales processes, and facilitating cross-functional collaboration throughout the opportunity lifecycle.
**Essential Functions**
+ Identify, research, and prospect potential clients aligned with strategic business objectives.
+ Generate, qualify, and prioritise leads by assessing customer needs, project requirements, strategic fit, and likelihood of conversion.
+ Support business development activities by identifying opportunities within existing and prospective customer accounts.
+ Maintain engagement with prospective clients and coordinate appropriate follow-up activities throughout the opportunity lifecycle.
+ Collaborate with Medical Affairs, Commercial, and other cross-functional teams to support customer engagement and business growth initiatives.
+ Support the management of opportunities throughout the sales lifecycle, from lead generation through proposal submission and contract execution.
+ Coordinate and support the development of proposals, RFPs, RFIs, capability presentations, and other customer-facing materials.
+ Assist with opportunity planning, resource coordination, project scoping, and the collection of information required for customer submissions.
+ Facilitate collaboration across functional teams to ensure timely, accurate, and high-quality deliverables.
+ Maintain accurate and up-to-date records within Salesforce and other business systems.
+ Track opportunities, customer interactions, sales activities, and key milestones throughout the sales cycle.
+ Support pipeline reviews, forecasting activities, and business performance reporting.
+ Produce regular reports and analyses on business development activity, opportunity status, and sales performance metrics.
+ Ensure data integrity and adherence to CRM best practices.
+ Provide operational, administrative, and business development support to the Medical Affairs team.
+ Assist with tracking customer engagements, project status updates, and key business metrics.
+ Support the preparation of presentations, business reviews, proposals, and customer-facing materials.
+ Collaborate with Medical Affairs leadership to support strategic initiatives and business growth objectives.
**General Responsibilities**
+ Maintain up-to-date knowledge of IQVIA services, therapeutic areas, and industry trends.
+ Build and maintain effective working relationships with internal stakeholders and external customers.
+ Perform other duties as assigned.
**Qualifications**
**Education**
+ Bachelor's Degree in Business, Life Sciences, Healthcare, Marketing, Management, or a related field preferred.
+ Equivalent combination of education, training, and experience will be considered.
**Experience**
1-3 years of experience in business development support, sales operations, lead generation, healthcare services, Medical Affairs, or a related commercial role preferred.
Experience working with CRM systems (Salesforce preferred) and sales pipeline management.
**Skills & Competencies**
+ Strong verbal and written communication skills.
+ Demonstrated ability to build relationships and engage professionally with internal and external stakeholders.
+ Strong organisational skills with the ability to manage multiple priorities simultaneously.
+ Analytical mindset with the ability to interpret data and provide actionable insights.
+ Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint, Outlook) and CRM platforms.
+ High attention to detail, accuracy, and follow-through.
+ Self-motivated with a proactive, positive, and collaborative approach.
+ Ability to work effectively in a fast-paced, cross-functional environment.
+ Strong problem-solving and project coordination skills.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at .
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**The Contract Analyst 1 - Job Description**
**Purpose:** Revise or develop contracts and related budgets and scope of work. Ensure the scope of work is defined correctly, budgets reflect the scope and any changes are integrated into the main study contract efficiently and accurately.
**Responsibilities:**
+ Works with the Project Management team and other internal stakeholders to develop budgets that include all current and projected costs in line with study scope
+ Majority of time spent collaborating with operational and finance team members to update and revise study budgets in Excel
+ Assist in the negotiation of legal contracting text using IQVIA Laboratories Contracting Policy, templates and fallbacks.
+ Develop and apply a working knowledge of the various IQVIA Laboratories business units to ensure proper contract terms for all types of studies Independently develop and review Agreements including Work Orders, GLSAs and Change Orders.
+ Lead negotiations for all assigned Agreements with moderate to high support
+ Follow up on outstanding contract and budget issues for resolution to meet internal and external deadlines and to minimize business and legal risk
+ May participate in process improvement initiatives intended to improve global delivery of contracts
+ Provide accurate updates on all outstanding contractual documents to management as required through required systems or tracking mechanisms
+ Primary customer interface on medium, complex contracts, responsible for developing and maintaining customer relationships
+ Assist/mentor peers including providing pre-submission review and approval of peer staff's documents in accordance with the Contract Management review guidelines, as assigned
+ Other duties as assigned
**Education/Qualifications: Recommended:**
+ BA or BS in business or life sciences (or equivalent experience)
+ 2 years in the pharmaceutical or CRO industry preferred with contract management related experience (or equivalent)
+ Demonstrated ability to plan, multi-task and prioritize
+ Demonstrated teamwork, communication and organizational skills
+ Required Proficiency in Excel and Word
+ Demonstrated problem solving skills
+ Excellent customer service skills, attention to detail and ability to be persistent while maintaining tact
+ Proven ability to work independently
+ Experience and comfort in a high volume, fast paced environment is essential.
+ Ability to negotiate
**Physical Requirements**
+ Extensive use of telephone and face-to-face communication requiring accurate perception of speech
+ Extensive use of keyboard requiring repetitive motion of fingers
+ Regular sitting for extended periods of time
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**As** **sociate / Associate Consultant - Global Advisory Services**
IQVIA is The Human Data Science Company, combining data, technology, advanced analytics, and human expertise to help healthcare clients improve outcomes for patients. Our solutions support better decision-making across the healthcare ecosystem and drive meaningful progress in life sciences.
**Commercial Solutions Excellence Centres (CSEC)**
CSEC is a global function that centralizes service delivery across IQVIA's core commercial offerings. It brings together global and regional teams to deliver scale, quality, efficiency, and innovation. By combining diverse talent with automation and AI, CSEC accelerates commercial excellence worldwide, working closely with global functions and regional business units to continuously improve delivery performance.
**Advisory Services**
Advisory Services is IQVIA's global consulting engine and a leading advisor to life sciences and healthcare clients. We support global and regional headquarters across the full product lifecycle, addressing complex commercial and access challenges. Our work spans brand and go-to-market strategy, pricing and market access, portfolio and asset strategy, launch excellence, commercial model design, digital health optimization, and omnichannel engagement.
We are a highly international team with a truly global way of working. Our culture emphasizes collaboration, analytical rigor, continuous learning, and practical impact. We leverage modern tools, standardized ways of working, and increasing use of automation and AI so our teams can focus on delivering meaningful outcomes for clients.
Joining Advisory Services offers a rewarding career in life sciences consulting, with exposure to diverse therapy areas, geographies, and business challenges. Team members collaborate with leading experts in pharma and healthcare, benefit from continuous learning, and contribute to innovative thinking shaping the future of healthcare.
**Role & Responsibilities**
Your analytical, inter-personal, critical thinking, business management and leadership skills will be called upon from day one. You will help create change in the world of Life Sciences, every project will be different but a sample of the accomplishments you can expect are:
+ Conducting primary and secondary research and performing quantitative and qualitative analysis to identify key client issues, translating the data into meaningful insights and communicating recommendations to key decision makers
+ Leveraging business experience and acumen in identifying strategic alternatives to client questions
+ Working in a team of like-minded professionals to create reports, presentations, workshops with client employees, management teams and other stakeholders, under the guidance our "the best on the business" team leaders
+ Developing broad knowledge of related consulting methodologies and pharmaceutical market through the delivery of consulting engagements and participation in formal and informal learning opportunities
+ Working independently and as part of a team, with responsibility for supervising junior team members
+ Assisting development and writing of proposals with senior support
+ Attending, supporting and presenting at client meetings
+ Contributing to learning, development and recruiting
**About You**
Candidates interested in joining as an Associate / Associate Consultant should have:
+ Undergraduate/master's degree in life sciences, economics/business, and 2/3 years' experience in the healthcare/pharmaceutical industry **OR** an academic PhD degree with commercial experience in the healthcare industry
+ Exceptional Master's degree or PhD in Sciences, Business Administration, or other related fields
+ 1-2 years previous experience in the life sciences industry and/or consultancy is a plus (Associate)
+ 2-4 years previous experience in the life sciences industry and/or consultancy (Associate Consultant)
+ Demonstrable analytical, interpretative and problem-solving skills
+ Previous experience in **Commercial Consulting, Strategy Consulting**
+ Well-developed written and verbal communication skills including presentations, meeting and workshop facilitation, business and report writing
+ Strong capability in juggling priorities to meet deadlines while retaining consistently high quality outcomes
+ Excellent interpersonal skills and ability to work effectively with others in and across the organization to accomplish team goals
+ Knowledge of key issues and current developments in the pharmaceutical and healthcare industries
+ An avid interest in the **healthcare** and **life sciences** industries
+ Knowledge of **consulting methodologies** , tools and techniques
+ Adaptability and an ability to learn quickly and apply new knowledge and thinking
+ A willingness and ability to travel
+ Right to work in the country you are applying for
**Important information:**
+ Location: Centurion
+ Right to work in the country of application
**What can you expect from our process:**
+ Step one: Starts with your application
+ Step two: Online test (business analysis and data interpretation)
+ Step three: Interview with our Talent Acquisition team
+ Step four: Interview with the business
+ 1st Round Fit interview and mini case study
+ 2nd Round Case Study
+ 3rd Round Competency Interview
+ Step five: Feedback
We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward.
**Whatever your career goals, we are here to ensure you get there!**
\#CONJAD
\#LI-KS2
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Clinical Lead, Global Study Leadership**
At IQVIA, our Clinical Leads play a critical role in bringing new medicines to patients faster. As part of the Global Study Leadership team, you'll lead the clinical delivery of international studies, partnering with Project Leads and cross-functional teams to ensure projects are delivered with quality, efficiency and a focus on improved patient outcomes. This is an exciting opportunity for experienced clinical research professionals looking to expand their global impact while advancing their careers in clinical trial leadership.
**Why Join Global Study Leadership?**
Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and customer-dedicated delivery units. You'll work across diverse therapeutic areas, including Oncology, Central Nervous System, Cardiovascular Renal Metabolic, Immunology, Respiratory, Infectious Disease, Rare Disease, Ophthalmology, Women's Health and Cell & Gene Therapy, while partnering with leading pharmaceutical and biotechnology companies around the world.
With structured career development, tailored training, mentorship, and opportunities to grow across Clinical, Project Management, Site Activation and Oversight roles, you'll build expertise that accelerates your career. Supported by a collaborative culture, flexible ways of working and a strong focus on work-life balance, you'll have the support to thrive both professionally and personally while helping bring new treatments to patients worldwide.
**What You'll Be Doing**
You'll drive the clinical delivery of global studies, ensuring projects meet quality, timeline, recruitment and budget objectives while maintaining compliance with applicable regulations, protocols and customer requirements. Working as part of an integrated cross-functional team, you'll collaborate with colleagues across functions, countries and regions to deliver high-quality studies, build global experience and support strategic customer engagements.
Key Responsibilities:
+ Leading the clinical delivery of global clinical research studies and projects
+ Driving patient recruitment strategies and supporting achievement of enrolment targets
+ Managing clinical risks and contributing to project risk mitigation plans
+ Ensuring clinical quality through oversight of compliance, quality standards and issue management
+ Managing clinical project finances, forecasting, scope changes and budget performance
+ Partnering with internal and external stakeholders to support successful project delivery
+ Supporting milestone achievement through effective planning, communication and team coordination
+ Leading and supporting clinical teams through resource planning, guidance and project-related training
+ Contributingto study governance, stakeholder reporting and operational decision-making .
**What We're Looking For**
+ Bachelor's degree in Life Sciences, Healthcare, or another scientific discipline
+ Typically requires 4 - 5 years of prior relevant clinical trial management experience,ideally within a CRO environment
+ Solid prior clinical research experience within monitoring, clinical operations, or study management
+ Strong knowledge of ICH-GCP, clinical trial conduct and regulatory requirements
+ Broad therapeutic and protocol knowledge
+ Strong communication, stakeholder management and problem-solving skills
+ Ability to manage competing priorities in a fast-paced global environment
+ Experience working across cultures and geographies
+ Financial awareness and understanding of clinical project delivery metrics
**Build Your Future with IQVIA**
If you're looking for a role that combines global exposure, clinical leadership, meaningful work and clear career progression, we'd love to hear from you. Join a team that partners with some of the world's most innovative healthcare organizations, leverages advanced technologies to enhance clinical trial delivery and plays a vital role in bringing life-changing treatments to patients worldwide while supporting your long-term career growth.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Job Overview**
Lead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout. Ensure that completion of work, clinical study management and project deliverables are on time and is in accordance with SOPs, policies and Good Clinical practices and applicable regulatory requirements. To provide CMS related support and assistance across multiple projects, sites and teams and review the structured clinical data output with access to medical charts. Adherence to protocol, overall completeness, and readiness of the supplied patient information to the next level of patient review and support the CMS leads in defining the metrics and timelines. Facilitate efficient and effective review of Site Visit Reports and assure consistent standards of implementation for quality to meet or exceed quality standards. Ensure subject safety, data integrity, escalation of issues and timely and responsive feedback in compliance with IQVIA SOP, ICH/ GCP guidelines, protocol requirements and regulatory compliance. Periodic review of site level KRIs and historic site performance according to Central Monitoring Plan.
**Essential Functions**
+ Review Central Monitoring KRIs, Endpoint Analyses, Quality Tolerance Limits (QTLs), and other analyses on an ad hoc basis or as outlined in the study-specific Central Monitoring Plan (CMP)
+ Minimum 1.5 yrs of Central Monitoring or Risk-based quality management Experience
+ Collaborate effectively with study team
+ Excellent Communication skills
+ Manage assigned sites and perform Subject Level Data Review independently for multiple studies, if required perform with both responsibilities as dual role.;
+ Perform remote monitoring visits for assigned sites as per requirement.;
+ Perform Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy (inclusion & exclusion criteria/ IP/AE/ Labs/EOT/EOS/ End points/SAEs etc.) Review any other information as necessary to determine overall readiness of the patient information for next level review.;
+ Perform Study specific analytics based on applicable study specific plans.; Contribute in developing new analytics proposal as per customer's demand, Ability to write analytical inferences to add business value and/or work on developing advanced analytics.;
+ Manage the operational insight of the assigned project(s) and complete the study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan, review, triage and action clinical study alerts, monitor clinical operation plan (COP) compliance etc.).;
+ - Provide Inputs to clinical study teams, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections.;
+ Adhere to customer roles and responsibilities or as activities defined per Scope Of Work
+ Support CMS leads to perform oversight on clinical deliverables on assigned projects as per the protocol, SOPs, respective regulation/guidelines and project Clinical Operations Plan.;
+ Collaborate and support project resources (CRAs/ CTAs/Centralized Monitoring team).;
+ Provide Mentorship to central monitors and CMA centralized monitoring associates.;
+ Act as subject matter expert on one or more CMS specific activities/deliverables.;
+ May lead study level efforts like automation of ISP, process enhancements, act as a POC for internal CM team and provide advice to the team.;
+ Perform the IP management for the assigned study to identify risk and proposed mitigation (including re-supply, re-labelling, Import/export licenses etc.).;
+ Ensure complete and accurate documentation of all the study specific tools and templates and keep the project audit ready.;
+ Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol, SOPs respective regulation and guidelines.;
+ Ensure accurate completion and maintenance of internal systems, databases, tracking tools/reports for the project specific information.;
+ Perform Management of triggers and preparation of i-site pack for respective sites and countries for assigned study(ies).;
+ Perform the activities delegated and/or act as back up for/to relevant stakeholders including leads within the project team.;
+ Conduct periodic review of site level KRIs and historic site performance according to Central Monitoring Plan and provide inputs to CMS leads to enable Early identification of site-level risk/issue(s).;
+ Monitor site performance and make recommendations for timely corrective actions (e.g. Site Telephone Contact or Triggered Onsite Monitoring Visit).;
+ Review the effectiveness of the recommended actions and take appropriate additional actions if no effect is observed.;
+ Work in accordance of the Study Central Monitoring Plan.;
+ Establish and maintain effective project/ site level communications with relevant stakeholders.;
+ Reviews reports per annotations, SOPs, guidelines etc., identifies issues and escalates the same to the Clinical Lead, prepares annotations and conducts CRA trainings, conducts monthly calls with relevant stakeholders to discuss major issues emerging from the trends noted during report review.;
+ Review daily reports and prepare weekly/monthly reports and present it to Leadership Team, need to mentor and provide appropriate trainings to associates and attend study team meetings as needed or requested.;
+ Act as a technical solution specialist (TSS) point of contact to connect with the project teams/internal stake holders for gathering the criteria and requirements.;
+ Analyze the complexity of the requirements and provide the EAC hours and turnaround time.;
+ Review of the Study Central Monitoring Plan
+ Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested
+ Adhere to the key activities outlined in the SOW as per customer requirements.
**Qualifications**
+ Bachelor's Degree Clinical, life sciences, mathematical sciences, or related field, or nursing qualification Req
+ Minimum of 3 years of relevant work experience or equivalent combination of education, training and experience.
+ Experience in clinical research field preferred. Pref
+ Good knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
+ Good Clinical system expertise.
+ Strong written and verbal communication skills including good command of English language.
+ Results and detail-oriented approach to work delivery and output.
+ Understanding of clinical/medical data.
+ Good motivational, influencing, coaching skills.
+ Ability to work on multiple projects and manage competing priorities. In depth therapeutic and protocol knowledge.
+ Strong organizational and problem-solving skills.
+ Effective presentation skills.
+ Demonstrated ability to deliver results to the appropriate quality and timeline metrics.
+ Ability to work across cultures and geographies with a high awareness and understanding of cultural differences and maintain effective working relationships with coworkers, managers and clients.
+ Extensive use of keyboard requiring repetitive motion of fingers.
+ Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
+ Regular sitting for extended periods of time.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Job Overview**
Lead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout. Ensure that completion of work, clinical study management and project deliverables are on time and is in accordance with SOPs, policies and Good Clinical practices and applicable regulatory requirements. To provide CMS related support and assistance across multiple projects, sites and teams and review the structured clinical data output with access to medical charts. Adherence to protocol, overall completeness, and readiness of the supplied patient information to the next level of patient review and support the CMS leads in defining the metrics and timelines. Facilitate efficient and effective review of Site Visit Reports and assure consistent standards of implementation for quality to meet or exceed quality standards. Ensure subject safety, data integrity, escalation of issues and timely and responsive feedback in compliance with IQVIA SOP, ICH/ GCP guidelines, protocol requirements and regulatory compliance. Periodic review of site level KRIs and historic site performance according to Central Monitoring Plan.
**Essential Functions**
+ Review Central Monitoring KRIs, Endpoint Analyses, Quality Tolerance Limits (QTLs), and other analyses on an ad hoc basis or as outlined in the study-specific Central Monitoring Plan (CMP)
+ Minimum 1.5 yrs of Central Monitoring or Risk-based quality management Experience
+ Collaborate effectively with study team
+ Excellent Communication skills
+ Manage assigned sites and perform Subject Level Data Review independently for multiple studies, if required perform with both responsibilities as dual role.;
+ Perform remote monitoring visits for assigned sites as per requirement.;
+ Perform Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy (inclusion & exclusion criteria/ IP/AE/ Labs/EOT/EOS/ End points/SAEs etc.) Review any other information as necessary to determine overall readiness of the patient information for next level review.;
+ Perform Study specific analytics based on applicable study specific plans.; Contribute in developing new analytics proposal as per customer's demand, Ability to write analytical inferences to add business value and/or work on developing advanced analytics.;
+ Manage the operational insight of the assigned project(s) and complete the study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan, review, triage and action clinical study alerts, monitor clinical operation plan (COP) compliance etc.).;
+ - Provide Inputs to clinical study teams, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections.;
+ Adhere to customer roles and responsibilities or as activities defined per Scope Of Work
+ Support CMS leads to perform oversight on clinical deliverables on assigned projects as per the protocol, SOPs, respective regulation/guidelines and project Clinical Operations Plan.;
+ Collaborate and support project resources (CRAs/ CTAs/Centralized Monitoring team).;
+ Provide Mentorship to central monitors and CMA centralized monitoring associates.;
+ Act as subject matter expert on one or more CMS specific activities/deliverables.;
+ May lead study level efforts like automation of ISP, process enhancements, act as a POC for internal CM team and provide advice to the team.;
+ Perform the IP management for the assigned study to identify risk and proposed mitigation (including re-supply, re-labelling, Import/export licenses etc.).;
+ Ensure complete and accurate documentation of all the study specific tools and templates and keep the project audit ready.;
+ Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol, SOPs respective regulation and guidelines.;
+ Ensure accurate completion and maintenance of internal systems, databases, tracking tools/reports for the project specific information.;
+ Perform Management of triggers and preparation of i-site pack for respective sites and countries for assigned study(ies).;
+ Perform the activities delegated and/or act as back up for/to relevant stakeholders including leads within the project team.;
+ Conduct periodic review of site level KRIs and historic site performance according to Central Monitoring Plan and provide inputs to CMS leads to enable Early identification of site-level risk/issue(s).;
+ Monitor site performance and make recommendations for timely corrective actions (e.g. Site Telephone Contact or Triggered Onsite Monitoring Visit).;
+ Review the effectiveness of the recommended actions and take appropriate additional actions if no effect is observed.;
+ Work in accordance of the Study Central Monitoring Plan.;
+ Establish and maintain effective project/ site level communications with relevant stakeholders.;
+ Reviews reports per annotations, SOPs, guidelines etc., identifies issues and escalates the same to the Clinical Lead, prepares annotations and conducts CRA trainings, conducts monthly calls with relevant stakeholders to discuss major issues emerging from the trends noted during report review.;
+ Review daily reports and prepare weekly/monthly reports and present it to Leadership Team, need to mentor and provide appropriate trainings to associates and attend study team meetings as needed or requested.;
+ Act as a technical solution specialist (TSS) point of contact to connect with the project teams/internal stake holders for gathering the criteria and requirements.;
+ Analyze the complexity of the requirements and provide the EAC hours and turnaround time.;
+ Review of the Study Central Monitoring Plan
+ Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested
+ Adhere to the key activities outlined in the SOW as per customer requirements.
**Qualifications**
+ Bachelor's Degree Clinical, life sciences, mathematical sciences, or related field, or nursing qualification Req
+ Minimum of 3 years of relevant work experience or equivalent combination of education, training and experience.
+ Experience in clinical research field preferred. Pref
+ Good knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
+ Good Clinical system expertise.
+ Strong written and verbal communication skills including good command of English language.
+ Results and detail-oriented approach to work delivery and output.
+ Understanding of clinical/medical data.
+ Good motivational, influencing, coaching skills.
+ Ability to work on multiple projects and manage competing priorities. In depth therapeutic and protocol knowledge.
+ Strong organizational and problem-solving skills.
+ Effective presentation skills.
+ Demonstrated ability to deliver results to the appropriate quality and timeline metrics.
+ Ability to work across cultures and geographies with a high awareness and understanding of cultural differences and maintain effective working relationships with coworkers, managers and clients.
+ Extensive use of keyboard requiring repetitive motion of fingers.
+ Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
+ Regular sitting for extended periods of time.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Job Overview**
Lead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout. Ensure that completion of work, clinical study management and project deliverables are on time and is in accordance with SOPs, policies and Good Clinical practices and applicable regulatory requirements. To provide CMS related support and assistance across multiple projects, sites and teams and review the structured clinical data output with access to medical charts. Adherence to protocol, overall completeness, and readiness of the supplied patient information to the next level of patient review and support the CMS leads in defining the metrics and timelines. Facilitate efficient and effective review of Site Visit Reports and assure consistent standards of implementation for quality to meet or exceed quality standards. Ensure subject safety, data integrity, escalation of issues and timely and responsive feedback in compliance with IQVIA SOP, ICH/ GCP guidelines, protocol requirements and regulatory compliance. Periodic review of site level KRIs and historic site performance according to Central Monitoring Plan.
**Essential Functions**
+ Review Central Monitoring KRIs, Endpoint Analyses, Quality Tolerance Limits (QTLs), and other analyses on an ad hoc basis or as outlined in the study-specific Central Monitoring Plan (CMP)
+ Minimum 1.5 yrs of Central Monitoring or Risk-based quality management Experience
+ Collaborate effectively with study team
+ Excellent Communication skills
+ Manage assigned sites and perform Subject Level Data Review independently for multiple studies, if required perform with both responsibilities as dual role.;
+ Perform remote monitoring visits for assigned sites as per requirement.;
+ Perform Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy (inclusion & exclusion criteria/ IP/AE/ Labs/EOT/EOS/ End points/SAEs etc.) Review any other information as necessary to determine overall readiness of the patient information for next level review.;
+ Perform Study specific analytics based on applicable study specific plans.; Contribute in developing new analytics proposal as per customer's demand, Ability to write analytical inferences to add business value and/or work on developing advanced analytics.;
+ Manage the operational insight of the assigned project(s) and complete the study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan, review, triage and action clinical study alerts, monitor clinical operation plan (COP) compliance etc.).;
+ - Provide Inputs to clinical study teams, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections.;
+ Adhere to customer roles and responsibilities or as activities defined per Scope Of Work
+ Support CMS leads to perform oversight on clinical deliverables on assigned projects as per the protocol, SOPs, respective regulation/guidelines and project Clinical Operations Plan.;
+ Collaborate and support project resources (CRAs/ CTAs/Centralized Monitoring team).;
+ Provide Mentorship to central monitors and CMA centralized monitoring associates.;
+ Act as subject matter expert on one or more CMS specific activities/deliverables.;
+ May lead study level efforts like automation of ISP, process enhancements, act as a POC for internal CM team and provide advice to the team.;
+ Perform the IP management for the assigned study to identify risk and proposed mitigation (including re-supply, re-labelling, Import/export licenses etc.).;
+ Ensure complete and accurate documentation of all the study specific tools and templates and keep the project audit ready.;
+ Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol, SOPs respective regulation and guidelines.;
+ Ensure accurate completion and maintenance of internal systems, databases, tracking tools/reports for the project specific information.;
+ Perform Management of triggers and preparation of i-site pack for respective sites and countries for assigned study(ies).;
+ Perform the activities delegated and/or act as back up for/to relevant stakeholders including leads within the project team.;
+ Conduct periodic review of site level KRIs and historic site performance according to Central Monitoring Plan and provide inputs to CMS leads to enable Early identification of site-level risk/issue(s).;
+ Monitor site performance and make recommendations for timely corrective actions (e.g. Site Telephone Contact or Triggered Onsite Monitoring Visit).;
+ Review the effectiveness of the recommended actions and take appropriate additional actions if no effect is observed.;
+ Work in accordance of the Study Central Monitoring Plan.;
+ Establish and maintain effective project/ site level communications with relevant stakeholders.;
+ Reviews reports per annotations, SOPs, guidelines etc., identifies issues and escalates the same to the Clinical Lead, prepares annotations and conducts CRA trainings, conducts monthly calls with relevant stakeholders to discuss major issues emerging from the trends noted during report review.;
+ Review daily reports and prepare weekly/monthly reports and present it to Leadership Team, need to mentor and provide appropriate trainings to associates and attend study team meetings as needed or requested.;
+ Act as a technical solution specialist (TSS) point of contact to connect with the project teams/internal stake holders for gathering the criteria and requirements.;
+ Analyze the complexity of the requirements and provide the EAC hours and turnaround time.;
+ Review of the Study Central Monitoring Plan
+ Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested
+ Adhere to the key activities outlined in the SOW as per customer requirements.
**Qualifications**
+ Bachelor's Degree Clinical, life sciences, mathematical sciences, or related field, or nursing qualification Req
+ Minimum of 3 years of relevant work experience or equivalent combination of education, training and experience.
+ Experience in clinical research field preferred. Pref
+ Good knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
+ Good Clinical system expertise.
+ Strong written and verbal communication skills including good command of English language.
+ Results and detail-oriented approach to work delivery and output.
+ Understanding of clinical/medical data.
+ Good motivational, influencing, coaching skills.
+ Ability to work on multiple projects and manage competing priorities. In depth therapeutic and protocol knowledge.
+ Strong organizational and problem-solving skills.
+ Effective presentation skills.
+ Demonstrated ability to deliver results to the appropriate quality and timeline metrics.
+ Ability to work across cultures and geographies with a high awareness and understanding of cultural differences and maintain effective working relationships with coworkers, managers and clients.
+ Extensive use of keyboard requiring repetitive motion of fingers.
+ Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
+ Regular sitting for extended periods of time.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Senior CRA 1 - Sponsor Dedicated**
**Gauteng based**
**Job Overview**
As a Sponsor-Dedicated Senior Clinical Research Associate I (Sr CRA I), you will be responsible for monitoring and managing clinical trial sites for a dedicated sponsor, ensuring studies are conducted in compliance with protocol requirements, Good Clinical Practice (GCP), applicable regulations, and sponsor expectations. This role offers the opportunity to work closely with a single sponsor, building strong partnerships and contributing to the successful delivery of clinical research programs.
**Key Responsibilities**
+ Conduct site selection, initiation, routine monitoring, and close-out visits.
+ Build strong relationships with study sites and support subject recruitment and enrollment activities.
+ Deliver study-related training and provide ongoing site support throughout the trial lifecycle.
+ Ensure protocol compliance, data quality, and adherence to regulatory requirements, escalating issues as needed.
+ Track study progress, including regulatory submissions, recruitment, data collection, and query resolution.
+ Maintain essential study documentation and ensure site files meet GCP and regulatory standards.
+ Prepare monitoring reports, follow-up communications, and other required study documentation.
+ Collaborate with cross-functional study teams to support successful project delivery.
+ Support study start-up, recruitment planning, and site financial activities, where applicable.
**Qualifications**
+ Bachelor's degree in Life Sciences, Healthcare, or related field preferred; equivalent combination of education and experience will be considered.
+ Minimum 2 years of independent on-site clinical monitoring experience.
+ Strong knowledge of GCP, ICH guidelines, and clinical research regulations.
+ Ability to assess and manage site performance, quality, and compliance.
+ Proficiency with Microsoft Office applications and clinical trial systems.
+ Excellent communication, organizational, problem-solving, and stakeholder management skills.
+ Ability to manage multiple priorities and work effectively in a fast-paced environment.
**Travel:** Frequent travel required based on study and business needs.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models.**
**Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!**
IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. _This is a remote/WFH position with all necessary equipment provided._
**What You'll Do**
+ Lead data management for complex, global clinical trials from study setup to database lock.
+ Serve as the main client contact for all data management deliverables.
+ Oversee SAE, PK, and external data reconciliation and database deployment.
+ Manage timelines, budgets, and resource allocation to meet customer expectations.
+ Mentor junior data management staff and promote best practices.
+ Drive process improvements and ensure regulatory and SOP compliance.
**Who We're Looking For**
Ideal candidates will have.
+ Bachelor's degree in life sciences, health, clinical, biological, or mathematical field.
+ No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.
+ Your previous roles/job titles may include _Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager_ .
+ Proven success managing large global studies (1000+ patients).
+ Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
+ Strong understanding of GCP, ICH, and clinical research processes.
+ Excellent communication and leadership skills.
**What IQVIA Offers**
+ Fully remote role - company equipment provided
+ Competitive salary and performance-based incentives
+ Career growth and learning opportunities through mentoring and internal mobility
+ Inclusive, global culture focused on innovation and collaboration
**What to Expect After Applying**
+ Recruiter video chat (20 min)
+ Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)
**Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare!**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled