Instagram
youtube
Facebook

Senior Manager, Pharmacovigilance

5+ 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

 

Senior Manager, Pharmacovigilance – Remote (UK/EU)

Job Summary:
Worldwide Clinical Trials is hiring a Senior Manager, Pharmacovigilance to oversee clinical drug safety operations in a fully remote role across the UK and EU. With a minimum of 5 years of pharmacovigilance experience, this is a leadership opportunity to manage staff, ensure regulatory compliance, and contribute to innovative global research within a leading mid-sized CRO.


Key Responsibilities:

  • Directly supervise pharmacovigilance staff and ensure PV compliance

  • Oversee project delivery in accordance with regulations and SOPs

  • Provide coaching, training, and performance feedback to team members

  • Manage pharmacovigilance timelines, scope, and budget awareness

  • Participate in proposal review, bid defence meetings, and SOP authoring

  • Support staff onboarding, recruitment, and ongoing development

  • Represent PV function in audits and client-facing interactions

  • Escalate project or performance issues as needed


Required Skills & Qualifications:

  • Bachelor’s degree in a life science, nursing, or equivalent field

  • Minimum 5 years of pharmacovigilance experience (pre-approval clinical trials)

  • Strong understanding of ICH-GCP, PV regulations, and safety data systems

  • Proficient in adverse event assessment and relational databases

  • Excellent communication and leadership skills

  • Experience supervising teams and guiding project execution

  • Ability to manage multiple projects with tight timelines

  • Fluent in written and verbal English

  • Willingness to travel for meetings or business development


Perks & Benefits:

  • 100% remote work from anywhere in UK or EU

  • Work in a collaborative, inclusive, and innovative CRO environment

  • Career progression in global pharmacovigilance leadership

  • Access to diverse clinical trial projects and sponsors

  • Opportunity to shape operational strategy and compliance

  • Supportive team culture with structured development programs


Company Description:

Worldwide Clinical Trials is a mid-sized, global Contract Research Organization (CRO) committed to improving patient outcomes through innovative, high-quality clinical research. With a team of over 3,500 professionals, we focus on bringing life-changing treatments to market while prioritizing collaboration, compliance, and excellence in execution.


Work Mode: Remote (UK/EU)


Call to Action:

Looking to take your pharmacovigilance career to the next level? Join Worldwide Clinical Trials and be part of global clinical development that saves lives. Apply now to make a difference in drug safety.