Associate II, Pharmacovigilance – Remote (UK/EU)
Employer: Worldwide Clinical Trials
Job Summary:
Worldwide Clinical Trials is seeking an experienced Associate II, Pharmacovigilance to join its global team remotely across the UK/EU. This critical role involves ensuring drug safety compliance, reviewing adverse event data, authoring safety documents, and maintaining regulatory alignment throughout the clinical development lifecycle. If you have a strong background in pharmacovigilance, clinical trials, and safety reporting, this is your chance to contribute to life-changing research in a collaborative CRO environment.
Key Responsibilities:
Author Safety Management Plans (SMPs) for assigned clinical studies
Review Serious Adverse Event (SAE) data for completeness and accuracy
Perform data entry and tracking in safety databases
Generate and follow up on queries for missing or unclear safety information
Conduct quality control (QC) checks of SAEs processed by other team members
Generate and submit regulatory safety reports (e.g., SUSARs, DSURs)
Maintain up-to-date knowledge of global PV regulations and guidance
Support safety submissions to IRBs, Ethics Committees, and Health Authorities
Required Skills & Qualifications:
Bachelor’s degree in a science-related field or nursing (or equivalent)
Minimum 1 year of pharmacovigilance experience in pre-approval clinical trials
Understanding of medical/scientific terminology and global safety regulations
Familiarity with safety databases and relational database systems
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
Excellent written and verbal communication skills
Strong attention to detail and organizational skills
Ability to manage competing priorities under tight timelines
Perks & Benefits:
Competitive compensation (specific salary not disclosed)
Remote work flexibility across the UK/EU
Inclusion in a diverse, supportive, and innovative team environment
Opportunities for career development within a global mid-size CRO
Equal opportunity employer with strong commitment to DEI
Access to comprehensive health, wellness, and work-life benefits (country-specific)
Company Description:
Worldwide Clinical Trials is a globally recognized mid-size Contract Research Organization (CRO) that partners with biotech and pharmaceutical companies to drive clinical development for some of the world’s most challenging diseases. The organization blends scientific excellence with innovation to deliver patient-focused results, with over 3,500 experts worldwide.
Work Mode:
Remote – Open to candidates in the UK and EU
Call to Action:
Are you ready to elevate your pharmacovigilance career in a globally respected CRO? Apply now to become part of the Worldwide Clinical Trials team and make an impact on global drug development and patient safety.
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