What Contract Research Organizations Jobs are in South Africa?

Showing 350 Contract Research Organizations jobs in South Africa

Lead Research Chemist (Organic Synthesis)

7646 Vlottenburg / Remote Placements24

Posted 9 days ago

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Job Description

full-time
About the Role Our client is seeking an accomplished Lead Research Chemist with expertise in organic synthesis to join their dynamic R&D team in Paarl, Western Cape . This leadership role will be responsible for designing and executing complex synthetic routes for novel compounds, mentoring junior chemists, and contributing to the strategic direction of our chemical research programs. The ideal candidate will possess a deep understanding of synthetic organic chemistry, a strong track record of innovation, and excellent problem-solving skills. This is an exceptional opportunity to lead impactful research within a well-resourced laboratory and contribute to the development of new products and technologies. We are committed to fostering a culture of scientific curiosity and excellence. Key Responsibilities
  • Lead the design and execution of multi-step organic synthesis projects to create novel molecules.
  • Develop and optimize synthetic methodologies for increased efficiency, yield, and purity.
  • Characterize synthesized compounds using a range of analytical techniques (NMR, MS, HPLC, GC).
  • Troubleshoot synthetic challenges and devise innovative solutions.
  • Mentor and guide junior chemists, providing technical expertise and direction.
  • Collaborate with cross-functional teams, including process development and analytical departments.
  • Author technical reports, research proposals, and contribute to patent applications and publications.
  • Maintain meticulous laboratory records and ensure compliance with safety and regulatory standards.
  • Stay abreast of the latest advancements in organic synthesis and related fields.
Requirements
  • Ph.D. in Organic Chemistry or a closely related field.
  • Minimum of 7 years of postdoctoral or industrial research experience in synthetic organic chemistry.
  • Proven track record of successfully designing and executing complex synthetic sequences.
  • Extensive experience with a wide array of modern organic reactions and purification techniques.
  • Proficiency in interpreting spectroscopic data (NMR, IR, MS) and chromatographic results.
  • Strong understanding of reaction mechanisms and stereochemistry.
  • Demonstrated leadership potential or experience in mentoring junior team members.
  • Excellent problem-solving skills, creativity, and attention to detail.
  • Strong written and verbal communication skills.
Benefits Our client offers a competitive salary, a comprehensive benefits package including health insurance and retirement contributions, and performance-based incentives. The role in Paarl, Western Cape is situated in a scenic region offering a high quality of life. Employees have access to state-of-the-art laboratory facilities and a collaborative research environment. Opportunities for professional development, including conference attendance and advanced training, are provided. We are dedicated to supporting employee growth and fostering a positive work-life balance.
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Senior Research Chemist (Organic Synthesis)

6001 Port Elizabeth / Remote Placements24

Posted 9 days ago

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Job Description

full-time
About the Role Our client, a leading innovator in specialty chemicals, is seeking a highly motivated Senior Research Chemist with expertise in organic synthesis to join their R&D team in Port Elizabeth . This role is crucial for driving the development of novel chemical compounds and improving existing synthesis pathways for a variety of industrial applications. You will be responsible for designing and executing complex multi-step organic synthesis, characterizing newly synthesized compounds, and contributing to the scale-up process. The ideal candidate will possess a strong theoretical background in organic chemistry, extensive practical laboratory skills, and a proven ability to solve challenging synthetic problems. This is an exciting opportunity to make significant contributions to chemical innovation within a dynamic and growing company located in the coastal city of Port Elizabeth . Key Responsibilities
  • Design and execute efficient and scalable synthetic routes for complex organic molecules.
  • Perform multi-step organic synthesis and purification techniques.
  • Characterize synthesized compounds using a variety of spectroscopic and analytical methods (e.g., NMR, MS, IR, HPLC).
  • Troubleshoot synthetic challenges and optimize reaction conditions.
  • Conduct literature searches and evaluate new synthetic methodologies.
  • Collaborate with process chemists to facilitate the scale-up of promising compounds from lab to pilot plant.
  • Maintain detailed and accurate laboratory records and prepare technical reports.
  • Ensure compliance with all safety regulations and laboratory best practices.
  • Mentor junior chemists and provide technical guidance.
  • Contribute to intellectual property generation through patent applications.
Requirements
  • Ph.D. in Organic Chemistry or a related field.
  • A minimum of 5 years of post-doctoral or industrial experience in organic synthesis.
  • Demonstrated expertise in modern organic synthesis techniques, including asymmetric synthesis and catalysis.
  • Proficiency in compound characterization techniques (NMR, MS, HPLC).
  • Strong understanding of reaction mechanisms and stereochemistry.
  • Experience with scale-up chemistry is a significant advantage.
  • Excellent problem-solving skills and a creative approach to synthetic challenges.
  • Strong written and verbal communication skills.
  • Ability to work independently and collaboratively within a research team in Port Elizabeth .
  • Commitment to safety and a proactive approach to risk management.
Benefits
  • Competitive salary and performance-based bonus opportunities.
  • Comprehensive medical, dental, and vision insurance.
  • Retirement savings plan with company matching.
  • Generous paid time off and holidays.
  • Opportunities for professional development, including conferences and training.
  • Access to advanced synthesis and analytical laboratory equipment.
  • A collaborative and innovative research environment.
  • Hybrid work flexibility to support work-life balance.
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Principal Research Chemist - Organic Synthesis

0299 Rustenburg / Remote Placements24

Posted 9 days ago

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Job Description

full-time
About the Role

Our client, a globally recognized leader in pharmaceutical research and development, is seeking a highly experienced and innovative Principal Research Chemist to join their esteemed organization in Rustenburg, North West . This senior position is crucial for driving the discovery and synthesis of novel drug candidates. The role involves leading complex organic synthesis projects, developing innovative synthetic routes, and contributing significantly to the early-stage drug discovery pipeline. The ideal candidate will possess exceptional expertise in synthetic organic chemistry, a deep understanding of medicinal chemistry principles, and a passion for advancing healthcare through scientific excellence. This position offers a remarkable chance to work at the forefront of pharmaceutical innovation within a collaborative and intellectually stimulating environment. The role is fully remote, allowing top-tier talent to contribute from anywhere.

Key Responsibilities
  • Lead the design and execution of complex multi-step organic synthesis projects to generate novel small molecule drug candidates.
  • Develop and optimize innovative synthetic methodologies and reaction conditions to improve efficiency and yield.
  • Apply expertise in medicinal chemistry to guide the design of molecules with desired pharmacokinetic and pharmacodynamic properties.
  • Characterize synthesized compounds using advanced analytical techniques (NMR, MS, HPLC, etc.) and interpret spectral data.
  • Collaborate effectively with biologists, pharmacologists, and other chemists to advance drug discovery programs.
  • Troubleshoot synthetic challenges and devise creative solutions to overcome obstacles.
  • Mentor and provide technical guidance to junior chemists and research associates.
  • Author comprehensive research reports, contribute to patent applications, and prepare manuscripts for publication in peer-reviewed journals.
  • Maintain a high level of productivity and manage multiple projects concurrently.
  • Stay abreast of the latest advancements in synthetic organic and medicinal chemistry.
Requirements
  • Ph.D. in Organic Chemistry or Medicinal Chemistry.
  • Minimum of 10 years of relevant experience in pharmaceutical or biotechnology R&D, with a significant portion focused on synthetic organic chemistry.
  • Proven track record of successful synthesis of complex organic molecules and a strong understanding of stereoselective synthesis.
  • Extensive experience with a wide range of modern synthetic techniques and reagents.
  • Proficiency in spectroscopic and chromatographic analytical techniques for compound characterization.
  • Deep understanding of structure-activity relationships (SAR) and structure-property relationships (SPR).
  • Demonstrated ability to lead research projects independently and work effectively in a team-oriented environment.
  • Excellent written and verbal communication skills, with strong presentation abilities.
  • Experience with computational chemistry tools and databases is a plus.
  • A strong publication record and/or patent filings are highly valued.
Benefits

Our client provides a highly competitive compensation package, including a substantial base salary, bonus potential, and stock options. Comprehensive health, dental, and vision insurance are provided, along with a generous retirement savings plan and life insurance coverage. This role offers significant opportunities for professional growth, including attendance at leading scientific conferences and access to advanced training programs. The fully remote nature of the role offers unparalleled flexibility and work-life balance. Our client is committed to fostering a culture of innovation and collaboration, providing a stimulating work environment where scientific contributions are recognized and rewarded. Employees also benefit from an employee stock purchase plan.

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Research Scientist - Synthetic Organic Chemistry

7600 Stellenbosch Placements24

Posted 6 days ago

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Job Description

full-time
About the Role Our client is a world-renowned pharmaceutical research company dedicated to discovering and developing life-saving medicines. We are seeking a talented and innovative Research Scientist with expertise in Synthetic Organic Chemistry to join our collaborative R&D team in **Stellenbosch, Western Cape**. This role is critical for the design and synthesis of novel small molecules with potential therapeutic applications. You will be responsible for executing multi-step organic syntheses, optimizing reaction conditions, and characterizing synthesized compounds using advanced analytical techniques. The ideal candidate possesses a strong foundation in modern synthetic methodologies, a meticulous approach to experimental design and execution, and a passion for contributing to drug discovery. This is an exceptional opportunity to work on cutting-edge research in a vibrant scientific community within **Stellenbosch, Western Cape**, contributing directly to the development of new pharmaceutical agents. Key Responsibilities
  • Design and execute complex, multi-step organic syntheses of novel small molecules.
  • Develop and optimize reaction conditions to improve yields, purity, and efficiency.
  • Purify synthesized compounds using techniques such as column chromatography, recrystallization, and preparative HPLC.
  • Characterize synthesized compounds using NMR spectroscopy, mass spectrometry, IR spectroscopy, and other relevant analytical techniques.
  • Troubleshoot synthetic challenges and devise creative solutions.
  • Maintain detailed and accurate laboratory notebooks and experimental records.
  • Collaborate effectively with medicinal chemists, biologists, and other team members to advance drug discovery projects.
  • Stay abreast of the latest advancements in synthetic organic chemistry and relevant scientific literature.
  • Contribute to the preparation of scientific reports, publications, and patent applications.
Requirements
  • Ph.D. in Organic Chemistry, Synthetic Chemistry, or a closely related field.
  • Proven experience in modern synthetic organic chemistry methodologies.
  • Hands-on experience with a wide range of organic reactions and purification techniques.
  • Proficiency in spectroscopic characterization techniques, particularly NMR and mass spectrometry.
  • Strong understanding of reaction mechanisms and stereochemistry.
  • Excellent problem-solving skills and a detail-oriented approach to research.
  • Ability to work independently and manage multiple synthetic projects simultaneously.
  • Strong communication and interpersonal skills for effective teamwork.
  • Experience in medicinal chemistry or process chemistry is a plus.
  • A passion for chemistry and its application in drug discovery.
Benefits Our client offers a competitive salary, comprehensive health and retirement benefits, and significant opportunities for professional development and career advancement within a leading pharmaceutical research organization. You will work in state-of-the-art laboratory facilities with access to advanced instrumentation. We provide a collaborative and intellectually stimulating work environment. The **Stellenbosch, Western Cape** location offers a high quality of life, surrounded by natural beauty and a thriving academic and scientific community.
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BI, Analytics & Data Insights Manager

Posted 5 days ago

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Job Description

Role Overview

A leading igaming and betting company is seeking a commercially focused, hands-on BI, Analytics & Data Insights Manager to lead the business intelligence, management information, reporting, and analytics capability across the organization.

This is not a pure enterprise architecture or theoretical governance role. The business already has technical architecture capability in place. The focus of this role is on transforming operational, customer, betting, gaming, financial, and marketing data into meaningful commercial insights that support faster, smarter business decision-making.

The successful candidate must be able to operate both strategically and operationally — engaging with leadership on business performance while also remaining close enough to the data, reporting environment, dashboards, and analytics outputs to ensure accuracy, usability, and commercial value.

This role is ideally suited to someone from an iGaming, sportsbook, online betting, fintech, payments, digital product, telecoms, or other high-volume transactional environments where real-time reporting, operational analytics, and customer behaviour insights are business critical.

Key Focus Areas

Business Intelligence & Reporting

  • Own and drive the BI and analytics capability across the business
  • Lead the development of operational, commercial, customer, financial, and executive dashboards
  • Ensure accurate, trusted, and actionable reporting across all departments
  • Deliver meaningful MI (Management Information) that supports strategic and operational decision-making
  • Improve visibility of business performance through self-service reporting and analytics
  • Standardise KPIs, reporting definitions, and dashboard structures across the organisation

Commercial & Operational Analytics

Drive analytics and reporting across areas including:

  • Sportsbook and casino performance
  • Customer acquisition, retention, churn, and player behaviour
  • CRM and campaign performance analytics
  • Revenue, GGR, NGR, bonus spend, and promotional effectiveness
  • Deposits, withdrawals, settlements, and payment trends
  • Operational and contact centre performance
  • Workforce and productivity reporting
  • Risk, fraud, AML, and responsible gambling indicators

The role requires someone who can identify trends, risks, opportunities, and operational inefficiencies through data analysis and translate these into commercially valuable insights.

Dashboarding, Visualisation & Data Storytelling

  • Design and oversee intuitive, executive-level dashboards and reporting environments
  • Ensure reporting is visually clear, commercially relevant, and user-friendly
  • Translate complex datasets into simplified business insights for non-technical stakeholders
  • Drive dashboard adoption across leadership and operational teams
  • Ensure near real-time visibility where operationally required

Data Integrity & Reporting Accuracy

  • Ensure consistency and integrity of reporting across betting, operational, finance, and CRM environments
  • Work closely with Finance and Operations to reconcile and validate key business metrics
  • Improve data quality, reporting reliability, and reporting governance
  • Support audit and compliance reporting requirements where needed
  • Identify reporting gaps and continuously improve analytics capability

Stakeholder Engagement

Partner closely with:

  • Executive leadership
  • Operations
  • Finance
  • Marketing & CRM
  • Customer Support
  • Compliance & Risk
  • Technology teams

The successful candidate must be commercially confident, highly collaborative, and capable of influencing business decisions through data-driven insights.

Technical Environment

Strong experience in several of the following is highly preferred:

  • Power BI
  • SQL
  • Excel / Advanced Excel
  • Data visualisation and dashboarding tools
  • Data warehousing / reporting environments
  • CRM and campaign analytics
  • Operational reporting environments
  • High-volume transactional databases
  • Near real-time reporting
  • Data modelling and KPI frameworks

Exposure to cloud analytics environments, customer data platforms, and iGaming reporting ecosystems would be advantageous.

Required Experience

Essential

  • 6+ years’ experience in BI, data analytics, reporting, or commercial insights roles
  • 3+ years in a senior BI or analytics management role
  • Experience within high-volume transactional environments
  • Strong hands-on dashboarding and reporting capability
  • Strong commercial analytics and business performance reporting experience
  • Advanced SQL and BI reporting exposure
  • Experience working with operational, financial, customer, or digital performance data

Highly Advantageous

  • iGaming, sportsbook, online betting, fintech, telecoms, or payments industry experience
  • Experience analysing customer/player behaviour and transactional data
  • Exposure to fraud, AML, responsible gambling, or risk analytics
  • Experience building reporting functions or BI capability within growing businesses

Personality & Working Style

The company is looking for someone who is:

  • Commercially sharp and analytically strong
  • Strategic but still hands-on
  • Naturally curious and insight-driven
  • Strong with detail and reporting accuracy
  • Calm in fast-paced operational environments
  • Able to communicate confidently with executives and operational teams alike
  • Passionate about using data to improve performance, efficiency, and customer experience

Why This Role Is Exciting

This is an opportunity to build and shape the BI and analytics capability within a rapidly growing digital gaming environment where data directly influences customer engagement, operational performance, revenue growth, and strategic decision-making.

The role offers strong visibility across the business and the opportunity to partner directly with leadership in driving a truly data-informed culture.

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Clinical Insights Analyst I

Remote Cytel

Posted 9 days ago

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Job Description

**Our values**
+ We believe in applying scientific rigor to reveal the full promise inherent in data.
+ We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
+ We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
+ We prize innovation and seek intelligent solutions using leading-edge technology.
1.Supports cross-functional study team and RBQM Leads in Protocol Risk Assessment, risk identification, and evaluation into Risk MAP.
2. Support RBQM Leads in selection and implementation of Key Risk Indicators (KRIs), and Quality Tolerance Limit parameters (QTLs) and other applicable assessments and dashboards, conducting end of trial summarization of risk management activities for inclusion to Clinical study report.
3. Drafts and oversee RBQM system set up specifications.
4. Perform the execution and review of the Study's assessments and analysis, and diagnosing and explaining anomalies identified in the data and risks.
5. Raise signal and issues in RBQM systems and raise actions as appropriate in RBQM system.
6. Delivers timely high-quality analytics and supporting RBQM leads in communication to the cross-functional study team to identify resolution.
7. Collaborate with assigned programmer to implement study-specific KRIs, QTLs, visualizations, and other analytics in the RBQM system.
8. Perform QC study setup in RBQM system vs RBQM system specifications, if required.
9. Act as RBQM programmer on set up of KRIs, QTLs, data quality assessments as well as visualizations in the RBQM system, if required.
10. Perform the maintenance of the Risk-Based Quality Management (RBQM) system based on RBQM Plan requirements, data sources and structure.
11. Ensure appropriate status and process documentation are produced and maintained during the study.
12. Communicate and/or escalate serious risks and issues to the RBQM Lead, study team and/or management and Quality, as needed.
13. Ensure inspection readiness for clinical risk management and centralized monitoring activities.
Proven experience in a clinical research environment, with experience in a pharmaceutical/biologics/biotechnology company.
Working knowledge of clinical development processes, understanding concepts and principles of study design, conduct and close out, as well as clinical program develop, and knowledge of clinical trials risk management concepts and principles in the Pharma or CRO industry.
Experience and understanding of Risk Based Monitoring system preferred.
Experience with data analytics and data visualization technologies.
Strong critical thinking and analytical skills and aptitude for data analytics including mathematical and statistical concepts.
High degree of accuracy and attention to detail.
Experience and understanding of clinical trial data from various sources (e.g., Clinical devices, SDTM, RAVE, IRT, etc).
Ability to work collaboratively in a team environment whilst managing changing priorities to achieve goals/targets.
Excellent English oral and written communication skills.
Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.
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Junior Quantity Surveyor

Posted 5 days ago

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Job Description

Overview of responsibilities:

Materials:

  • After the first quote is approved, create & check specifications to main contract quote & contract.
  • Analyse tender drawings and check for errors, then suggest to draughting department the appropriate changes. For example, details, materials, quantities, etc.
  • Take off and measure buildings in great detail in order to get exact material requirements. This is done according to specific measuring spreadsheets.
  • Compare costing to material measured in terms of quality vs quality vs cost.
  • Compile a comprehensive Material / Loading Schedule of all materials
  • Distribute material schedules to purchasing department, site managers & factory.
Sub-Contractors
  • Source quotes for sub-contracting items and negotiate on price where possible.
  • Ensure Quotes procured are comprehensive in including all of the works required to be executed under the Sub contract
  • Ensure sub-contractors are suitably skilled, experienced and qualified to carry out the works required.
  • Ensure the terms of appointment are clear to the sub-contractor in terms of Payment schedule, Retentions, Quality and performance required.
  • Ensure Sub-contractors are appointed on price within the cost allowable.
  • Update and maintain preferred sub-contractor database
  • Negotiate with sub-contractors and create purchase orders.
  • Source and one-off Sub-Contractors needed for a project or for late notifications.
  • Handover relevant documents to Site Manager before or during contracts meeting

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Senior Statistical Programmer

Posted 9 days ago

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Job Description

Senior Statistical Programmer - Client Based
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We're looking for a talented Senior Statistical Programmer to become a key contributor within our diverse, collaborative, and forward‑thinking team. At ICON, you'll play an integral role in transforming clinical trial data into meaningful insights that drive critical decision‑making in global healthcare.
In this role, you'll take ownership of developing and validating high‑quality statistical programs, partnering closely with expert biostatisticians, and ensuring our outputs meet the highest scientific and regulatory standards. Your expertise will directly support the success of our clinical studies and the advancement of life‑changing therapies.
**What You Will Be Doing**
+ Designing, developing, and validating SAS programs to support statistical analysis and reporting of clinical trial data.
+ Collaborating with biostatisticians to shape analysis plans, identify appropriate methodologies, and deliver reliable insights.
+ Conducting comprehensive quality control checks to ensure the accuracy, consistency, and integrity of statistical outputs.
+ Supporting the creation of statistical reports, presentations, and regulatory submission documentation.
+ Identifying opportunities to enhance programming processes, contributing to continuous improvement and innovation within the team.
**Your Profile**
+ Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related discipline.
+ Proven experience in statistical programming, ideally within clinical research or the pharmaceutical industry.
+ Strong command of SAS programming, with a solid grounding in statistical concepts and clinical data analysis.
+ Exceptional analytical and problem‑solving abilities, with meticulous attention to detail.
+ Effective communicator with strong teamwork skills and the confidence to translate complex analyses into clear, actionable insights.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
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Senior Clinical Data Science Programmer

Posted 9 days ago

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Job Description

Senior Clinical Data Science Programmer (Clinical SAS Listings)
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Are you an experienced **Clinical SAS Listings Programmer** with 3+ years of experience developing and maintaining clinical study listings looking for your next opportunity?
ICON is growing and we're looking for talented professionals to join our Clinical Data Science team in a fully remote role. This is an exciting opportunity for an experienced programmer with strong expertise in **Clinical Study Listings, including DM Listings and Reconciliation Listings** , to work in a client-facing role and deliver high-quality clinical data science and programming solutions that support clinical development programmes across a global portfolio.
**What You Will Be Doing**
+ Develop, validate, and maintain Clinical Study Listings, including DM Listings, Reconciliation Listings, and other study-specific listings.
+ Ensure study listings are configured, delivered, and maintained in line with agreed timelines and quality expectations.
+ Manage clinical study listings in compliance with clinical standards to support the successful execution of clinical trials.
+ Serve as the subject matter expert for Clinical Study Listings, providing support, troubleshooting, and maintenance activities.
+ Partner directly with stakeholders, providing technical expertise and acting as a key contact for programming-related activities.
+ Participate in client meetings, delivering updates, presenting outputs, and supporting decision-making throughout the study lifecycle.
+ Provide guidance on programming best practices, coding standards, validation approaches, and data quality controls.
**You Will Have/Be**
+ Bachelor's degree in Life Sciences, Computer Science, Statistics, or a related discipline.
+ Minimum 3 years of experience developing, validating, and maintaining Clinical SAS Listings.
+ Demonstrated experience producing DM Listings, Reconciliation Listings, and other clinical study listings.
+ Strong proficiency in SAS and experience with programming languages such as R, Rave Custom Functions, and Python.
+ Understanding of CDISC standards and clinical reporting best practices.
+ Excellent verbal and written communication skills.
+ Ability to work independently in a remote environment while managing multiple priorities and deadlines.
\#LI-RD1
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
Is this job a match or a miss?
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Pest Control Officer, George

Posted 5 days ago

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Job Description

Overview of responsibilities
  • Work to company standards by completing tickets on time at all clients sites.
  • Ensure the service and information is scanned and documented on the Pest Management System
  • Provide a professional and comprehensive service in line with SOPs
  • Supervise and teach PCO assistants and Interns in line with SOP and clients scope of work and/or HACCP standards as required
  • Take care of company vehicle and equipment
Documentation:
  • Complete daily treatments reports and ensure IPM file is maintained and updated after each service
  • Obtain clients signature after service is completed
  • Document proofing and housekeeping requirements
  • Document all units missing and / or broken
Ensure Health and Safety protocols are followed
  • Apply and implement all safety standards
Customer Care
  • Build professional relationships with all stakeholders
  • The successful candidate must demonstrate a high level of commitment to customer service, as delivering exceptional service is the branchs top priority and primary focus.
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