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Associate Ii, Pharmacovigilance

1+ years
Not Disclosed
10 July 16, 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

 

Associate II, Pharmacovigilance – Remote (UK/EU)

Job Summary:
Worldwide Clinical Trials is hiring a Pharmacovigilance Associate II to support global clinical trial safety initiatives in a fully remote role across the UK and EU. If you have at least 1 year of pharmacovigilance experience and a passion for improving patient safety, this role offers the opportunity to work across multiple therapeutic areas and engage with international regulatory authorities.


Key Responsibilities:

  • Author Safety Management Plans (SMPs) for assigned studies

  • Attend internal and client meetings

  • Review Serious Adverse Events (SAEs) for completeness and accuracy

  • Perform data entry in Safety Database and track incoming safety data

  • Generate safety queries and follow up with investigational sites

  • Perform Quality Control (QC) on SAEs processed by team members

  • Prepare and submit periodic safety reports and regulatory submissions

  • Stay current on international PV regulations and guidelines


Required Skills & Qualifications:

  • Bachelor’s degree in life sciences, nursing, or a related field

  • Minimum 1 year of pharmacovigilance experience, especially in pre-approval clinical trials

  • Familiarity with medical terminology and adverse event assessment

  • Strong knowledge of Microsoft Office (Word, Excel, PowerPoint)

  • Attention to detail and ability to manage multiple tasks under tight deadlines

  • Excellent communication and collaboration skills

  • Knowledge of safety database systems and global safety regulations


Perks & Benefits:

  • Fully remote working opportunity across UK/EU

  • Work-life balance with flexible scheduling

  • Inclusive and diverse workplace culture

  • Opportunities for global collaboration and cross-functional exposure

  • Career advancement through structured development paths

  • Contribution to clinical development of life-saving therapies


Company Description:

Worldwide Clinical Trials is a global, mid-sized Contract Research Organization (CRO) with over 3,500 professionals committed to transforming the clinical research experience. We specialize in drug safety, regulatory compliance, and full-spectrum clinical trial services across therapeutic areas, helping to bring new treatments to patients faster.


Work Mode: Remote (UK/EU)


Apply Now:

Are you ready to make an impact in global drug safety? Join our dedicated PV team and be part of life-changing research. Apply today to become a part of Worldwide Clinical Trials' mission to advance healthcare innovation.