Pharmacovigilance Associate II – Remote (UK/EU)
Employer: Worldwide Clinical Trials
Location: United Kingdom | Remote
Salary: Competitive
Start Date: 2 July 2025 | Closing Date: 1 August 2025
Job Summary:
Worldwide Clinical Trials is hiring a Pharmacovigilance Associate II for a fully remote role within the UK/EU region. In this dynamic role, you'll support safety operations by managing serious adverse event (SAE) data, authoring safety plans, and ensuring compliance with global pharmacovigilance regulations. This is a perfect opportunity for those looking to grow in drug safety while contributing to the full lifecycle of clinical drug development.
Key Responsibilities:
Draft Safety Management Plans (SMP) for assigned clinical studies
Attend internal and sponsor/client meetings
Review SAE reports for accuracy and completeness
Perform SAE data entry and maintain tracking logs in safety databases
Query and follow up on missing or unclear adverse event data
Conduct QC of SAE cases processed by team members
Generate regulatory safety reports and manage safety submissions
Prepare periodic safety update reports (PSURs) as needed
Stay updated with evolving pharmacovigilance guidelines and regulatory changes
Required Skills & Qualifications:
Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field
Minimum 1 year of experience in pharmacovigilance within clinical trials (pre-approval)
Strong knowledge of global PV regulations and AE/SAE case management
Familiarity with safety databases and relational data systems
Proficiency in MS Office tools (Excel, Word, PowerPoint)
Detail-oriented with strong analytical and problem-solving abilities
Excellent verbal and written communication skills
Proven ability to handle multiple priorities in a fast-paced environment
Perks & Benefits:
Fully remote work model (UK/EU-based)
Competitive compensation package
Inclusive and diverse work culture
Opportunity to contribute to global drug development
Access to cutting-edge clinical research technology
Supportive leadership with growth-focused initiatives
Annual leave, retirement planning options, and healthcare benefits
Company Description:
Worldwide Clinical Trials is a mid-sized global Contract Research Organization (CRO) committed to transforming clinical research through innovation, quality, and excellence. With over 3,500 professionals worldwide, we bring a personalized, high-touch approach to clinical trial execution—especially in drug safety and pharmacovigilance.
Work Mode:
Remote (UK/EU)
Call to Action:
Ready to make a global impact in pharmacovigilance? Apply now to join Worldwide Clinical Trials and shape the future of drug safety while working remotely from anywhere in the UK or EU.
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