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Associate Ii, Pharmacovigilance

1+ years
Not Disclosed
10 July 18, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

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.