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Senior Pharmacovigilance Associate

2+ years
Not Disclosed
10 Dec. 31, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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 Pharmacovigilance Associate
Location: Guildford, UK
Employment Type: Full-time
Department: ICSR Management
Company: PrimeVigilance (part of Ergomed PLC)


Company Description

PrimeVigilance, part of Ergomed PLC, is a leading pharmacovigilance service provider established in 2008. With teams based across Europe, North America, and Asia, we offer specialized services in Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance.

We are proud of our global growth and the strong, long-lasting relationships we maintain with pharmaceutical and biotechnology companies, spanning all therapy areas including medical devices.

At PrimeVigilance, we believe in investing in our people and providing an excellent training and development platform. We prioritize employee well-being, mental health, and work-life balance, fostering an environment that promotes high-quality service and satisfaction.

Join us in our mission to make a positive impact on patients’ lives!


Job Description

We are looking for a Senior Pharmacovigilance Associate with a life science or biomedical background (chemistry, biology, biotechnology, veterinary science, etc.). This role is an exciting opportunity for new graduates to begin and develop their career in drug safety. As part of a project team, you will contribute to pharmacovigilance activities on behalf of PrimeVigilance.

You will have the chance to work on teams of varying sizes, from small clinical trials to large-scale post-marketing teams. We seek proactive and motivated individuals who strive to surpass set targets.

Responsibilities:

  • Process Individual Case Safety Reports (ICSRs) from all sources (post-marketing and clinical trials) following applicable regulations, PrimeVigilance procedures, and client-specific requirements.
  • Focus on triage, data entry, quality review, and submission workflow steps.
  • Conduct reconciliation activities for all types of received reports.
  • Work under supervision and mentoring from more experienced colleagues.

Qualifications:

  • Life science or biomedical background (e.g., chemistry, biology, biotechnology, veterinary science). Previous experience is not required.
  • Enthusiastic about learning and contributing to patient safety.
  • Strong organizational, multitasking, and time management skills, with excellent attention to detail.
  • Strong interpersonal and communication skills.
  • Advanced English skills (B2 level or higher), both verbal and written.

Why PrimeVigilance?

At PrimeVigilance, we value diversity, equity, and inclusion, and strive to create an equal opportunities workplace. Our people are our greatest strength, and we work together to improve the lives of those around us.

What we offer:

  • Internal training and career development opportunities.
  • A strong emphasis on personal and professional growth.
  • A friendly, supportive working environment.
  • Opportunities to work with colleagues across the globe, with English as the company language.

Our core values—Quality, Integrity & Trust, Drive & Passion, Agility & Responsiveness, Belonging, and Collaborative Partnerships—are fundamental to how we operate. If these values resonate with you, PrimeVigilance is the right place to grow your career.