Job Title:
Associate II, Pharmacovigilance
Location:
Remote – United Kingdom / European Union
Company:
Worldwide Clinical Trials
Compensation:
Competitive (not specified in the job description)
Job Summary
Worldwide Clinical Trials is seeking a Pharmacovigilance Associate II to support drug safety efforts in a fully remote role available across the UK and EU. Ideal candidates will have at least 1 year of pharmacovigilance experience in pre-approval clinical trials, strong medical terminology understanding, and familiarity with global safety regulations. Join a mission-driven, mid-sized CRO known for innovation and excellence in clinical development.
Key Responsibilities
Author Safety Management Plans (SMPs) for assigned studies
Participate in internal and client meetings, including Investigator Meetings
Review Serious Adverse Event (SAE) data for completeness and accuracy
Perform data entry in the Safety Database and maintain safety tracking systems
Generate and follow up on safety-related queries to sites
Perform QC of SAEs processed by fellow PV Associates
Prepare and submit periodic and regulatory safety reports
Ensure compliance with international safety regulations and guidelines
Required Skills & Qualifications
Bachelor’s degree in science, nursing, or related field
Minimum 1 year of experience in pharmacovigilance (clinical trials – pre-approval)
Solid understanding of medical/scientific terminology and adverse event assessment
Familiarity with international PV reporting requirements (e.g., ICH-GCP, GVP)
Experience with safety databases and data extraction
Strong communication and documentation skills
Proficiency in MS Office (Word, Excel, PowerPoint)
Highly organized with the ability to prioritize multiple tasks
Adaptable, dependable, and detail-oriented team player
Perks & Benefits
Fully remote work from anywhere in the UK or EU
Inclusive, diverse workplace culture with global collaboration
Be part of a high-impact team that advances drug safety globally
Opportunities for training, mentorship, and professional growth
Work with cutting-edge CRO technology and global regulatory processes
Company Description
Worldwide Clinical Trials is a leading midsize CRO with over 3,500 professionals worldwide, delivering scientifically-driven clinical development services. Renowned for its innovation and flexibility, the company partners with biopharma clients to accelerate drug development and improve patient outcomes across therapeutic areas.
Work Mode
Remote – United Kingdom / European Union
Call-to-Action
Ready to advance your pharmacovigilance career in a global CRO environment? Join Worldwide Clinical Trials and help bring life-saving therapies to market. Apply now to make your impact in global drug safety.
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