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Our ever-growing **Lifecycle Safety Medical** team is expanding. The role participates in all aspects of the Medical Safety activities as per scope of work. This includes, but is not limited to providing and maintaining of PV and risk management expertise to internal and external stakeholders, maintaining knowledge relevant to allocated product portfolios, conducting medical evaluation of post-marketing adverse drug reactions, review and contribution to signal management and benefit-risk evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to responses to questions from health authorities, reviewing and contributing to periodic aggregate reports, contributing to safety review of study protocols, investigators brochure and other reference safety information, and serving as an internal consultant for any medical support for pharmacovigilance operations.
Associate Medical Safety Director
Role responsibilities:
+ Providing aggregate reviews of safety information, including clinical data, to maintain oversight of a product's safety profile
+ Leads signal detection and analysis, including, signal detection strategy, frequency, and timing, reviews the Signal Detection Reports and other sources of data as applicable, raises potential signals for team discussion, contributes to safety analysis reports presentations of signal evaluation data as appropriate
+ Providing medical review and contribution to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports
+ Providing medical review and contribution to Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies
+ Review and contribute to benefit-risk evaluation of drugs in clinical trial and post marketing set up
+ Providing safety oversight and contribution for label development, review, and updates
+ Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document
+ Performing medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summary and serve as an internal consultant to pharmacovigilance case processing teams
+ Representing safety and clinical data review findings during internal and external stakeholder meetings
+ Providing medical safety support, contribution, and attendance at Safety Governance and other Meetings as needed
Do you have the skills, experience and qualification required for the role:
+ A medical degree from an accredited and internationally recognized medical school
+ Around three years of clinical practice experience with two additional years in the pharmaceutical or associated industry, or equivalent combination of education, training and required experience
+ Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice and clinical trials and pharmaceutical research process
+ Maintain knowledge of assigned product portfolio, therapeutic area, and recent literature
+ Experience in Signal detection, Aggregate reports and Risk management.
+ Capability to synthesize and critically analyze data from multiple sources and communicate complex clinical issues and analyses orally and in writing
+ Ability to establish and meet priorities, deadlines, and objectives
+ Demonstrated skills in contributing to multiple assignments required, capacity to work under pressure as well as initiative and flexibility and ability to adapt to changing business needs
+ Ability to establish and maintain effective working relationships with coworkers, managers, and clients, including mentorship if needed
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

**Duties/Responsibilities:**
+ Act as signal detection and literature lead, or back-up lead to contribute to the conduct of ongoing literature safety surveillance for marketed and investigational products, evaluating events of special interests as well as aggregate data review
+ Author and finalize aggregate reports, including but not limited to PBRERs/PSUR, DSURs and ACOs.
+ Author responses to regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required.
+ Can serve as principal owner (molecule lead) for the molecule and have responsibility for completion of the deliverable and in compliance with all applicable Key performance indicators (KPI); Set-up and update products' signaling strategies, as approved by the customer's Safety Strategy Lead. Author and/or QC review all types of signal management deliverables. Lead/ conduct ongoing signal detection activities as per agreed signaling strategies, perform signal validation and signal evaluation analyses for proactive and timely identification of signals and characterization of risks, as approved by the customer's Safety Strategy Lead. Responsible for full documentation and tracking of signals.
+ Ensuring the completion of molecule deliverables on time and liaise with portfolio clinical science scientists, service provider process leads and cross-functional stakeholders.
+ Distribution of molecule work within team consisting of molecule scientists, when necessary, coordinating support across molecules and disease areas when there are peaks and troughs in workload.
+ End-to-end molecule work oversight and responsibility (i.e., ensuring consistent tracking of signals from detection to assessment to inclusion in aggregate reports).
+ Ensuring an in-depth knowledge of the molecule and disease area within the service provider molecule team.
+ Oversight and responsibility of quality-of molecule deliverables to the customer's molecule team, with "hands-on" involvement, i.e., involved in authoring DSR conclusion, participating in SD/Lit meetings between service provider and customers.
+ Responsible for resolution of issues on molecule deliverables (if necessary, in collaboration with service provider process lead).
+ Participate in internal and external audits and inspections, as required.
+ Read, acknowledge and adhere to all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion to maintain compliance and documented
+ Conduct regular lessons learned with the working teams to ensure all information from the customer is cascaded to the relevant team members.
**Qualifications:**
+ Life science graduate/post-graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance
+ 4-6 years of relevant experience in Pharmacovigilance including hands-on experience of drug safety, aggregate reports, signal detection/signal management preferred
+ Excellent communication (written and verbal) skills
+ Team working
+ English - fluent (spoken, written)
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

Key Responsibilities:

• Perform planned and breakdown maintenance on plant equipment
• Fault-find across electrical, mechanical, and pneumatic systems
• Carry out routine inspections and preventative maintenance schedules
• Repair and replace motors, pumps, conveyors, gearboxes, and general plant machinery
• Basic electrical fault-finding (motors, panels, wiring)
• Complete job cards, maintenance logs, and safety documentation
• Ensure compliance with health, safety, and quality standards

Requirements:

• Trade tested (Millwright/Fitter/Electrician or equivalent) advantageous
• Strong all-round maintenance & troubleshooting experience
• Industry background in Food/FMCG or heavy industry/mining
• Willingness to work shifts/standby as required
• Valid driver's license advantageous

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Key Responsibilities:

• Oversee daily site construction activities, ensuring full compliance with safety regulations, quality standards, and permit-to-work procedures.
• Independently complete Risk Assessments, Method Statements, and other HSE documentation.
• Manage and coordinate the construction team, including supervisors, team leaders, and subcontractors.
• Prepare and submit daily site progress reports, ensuring all project documentation is accurate and up to date.
• Interpret engineering drawings, technical specifications, and project plans.
• Plan, schedule, and monitor construction progress against project timelines and milestones.
• Coordinate with engineering, HSE, and project management teams to resolve on-site technical issues, delays, or constraints.
• Order, control, and manage site materials, tools, and equipment.
• Attend and conduct site meetings with engineers, clients, and project stakeholders.
• Demonstrate strong BOQ understanding, including quantity verification and tracking.

Minimum Requirements:
- Degree or Diploma in relevant Field.
- At least 2 years experience in construction or site management roles.
- Ability to work under pressure and meet deadlines.
- Advantageous: Experience working on petrochemical or industrial projects, and HSE or construction-related certifications.

Minimum Requirements:

• PSIRA registered (Grade C preferred)
• Proven experience installing and servicing alarm systems
• Experience with CCTV installation and monitoring systems
• Good fault-finding and troubleshooting skills
• Valid driver's licence advantageous
• Reliable, professional, and customer-focused

Duties:

• Install, service, and maintain alarm and CCTV systems
• Diagnose and repair system faults
• Conduct routine maintenance and testing
• Complete installation and service reports
• Provide professional customer service

Only candidates with relevant technical security systems experience will be considered.