Job Title: Senior Associate, Pharmacovigilance
🏢 Employer: Worldwide Clinical Trials
📍 Location: United Kingdom | Remote (Homeworking)
💰 Salary: Competitive
📅 Start Date: 17 September 2025
⏳ Closing Date: 17 October 2025
About Worldwide Clinical Trials
We are a global, midsize CRO with 3,500+ experts worldwide. At Worldwide, we push boundaries, innovate, and take creative approaches to accelerate the path to cures for some of the world’s most persistent diseases.
Our mission is simple: work with passion and purpose to improve lives. We value diversity, inclusivity, and collaboration, creating an environment where people thrive by being themselves.
Pharmacovigilance at Worldwide
Pharmacovigilance is central to ensuring drug safety throughout the lifecycle of a compound — from First-in-Human administration to global regulatory approval.
Our PV team:
Reviews and analyzes global safety events.
Partners with clients to ensure compliance with regulators, investigators, ethics committees, and IRBs.
Plays a vital role in clinical drug development.
Key Responsibilities
Author Safety Management Plans for assigned studies.
Attend internal/client meetings and present at Investigator Meetings.
Review incoming Serious Adverse Event (SAE) data for accuracy and completeness.
Enter safety data into databases and track safety information.
Generate queries for missing/unclear data and follow up with sites.
Perform quality control (QC) of SAEs processed by other PV Associates.
Prepare and submit regulatory safety reports and periodic safety updates.
Maintain knowledge of safety regulations and guidelines.
Track budget and scope of work, escalating scope changes when needed.
Contribute to bid defences and presentations.
Mentor/train new PV staff.
Perform additional assigned duties.
What You Bring
Strong knowledge of medical/scientific terminology, adverse event assessment, global safety regulations, and reporting requirements.
Proficiency in safety database systems and data extraction.
Excellent organizational skills with ability to manage multiple priorities under tight timelines.
Strong problem-solving and decision-making skills.
Professional, diplomatic communication in a global environment.
Ability to receive/provide feedback constructively.
Experience & Qualifications
🎓 Education: Bachelor’s degree in a science-related field, nursing, or equivalent.
🧪 Experience: Minimum 5 years in pharmacovigilance (clinical trials, pre-approval).
💻 Technical Skills:
MS Office (Excel, PowerPoint, Word).
Safety database management.
✍️ Communication: Excellent written and verbal English.
🌍 Other:
Independent and effective in matrix environments.
Willingness for limited travel (domestic & international).
Why Join Worldwide?
Be part of a mission-driven CRO shaping the future of drug development.
Work in a collaborative, global team with hands-on leadership.
Thrive in a supportive, inclusive workplace that values your growth.
Make a real impact on patients and caregivers worldwide.
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Atlanta | Augusta | Rome |Maine :
Bangor | Brewer |New Jersey :
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Boulder | Denver | Westminster |Connecticut :
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Duluth | Eden Prairie | Fridley | Hibbing | Maple Grove | Minneapolis and St. Paul, Minnesota. | Minnetonka | St.Paul |Kentucky :
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Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
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Arkansas | Remote Australia |New South Wales :
Ballina | Sydney |Republic of Western Australia :
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South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
Harrogate |South Yorkshire :
Sheffield |Oxfordshire :
Witney |Ontario :
Uxbridge | North York | Renfrew | Mississauga | Australia | Richmond Hill |Canada :
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Tallinn |Hà Nội :
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Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
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Lyon | Paris |South Africa :
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Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
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