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Associate Ii, Pharmacovigilance - Uk/Eu - Remote

1+ years
Not Disclosed
10 July 3, 2025
Job Description
Job Type: Full Time 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

 

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.