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Pv Associate

0-2 years
Not Disclosed
10 Nov. 20, 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

Join PrimeVigilance – Start Your Career in Pharmacovigilance

About Us
We are PrimeVigilance, part of the Ergomed Group, a specialised mid-sized pharmacovigilance service provider established in 2008. Over the years, we have achieved consistent global growth with a team spanning Europe, North America, and Asia. Our services cover Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance, supporting pharmaceutical and biotechnology partners worldwide.

As one of the leaders in our field, we pride ourselves on long-lasting partnerships and first-class service. Covering all therapy areas, including medical devices, we also invest heavily in our staff's training and development. We believe in fostering employee well-being and work-life balance, ensuring high-quality service delivery in an inclusive, supportive environment.

Join us in our mission to make a meaningful impact on patients' lives.


Job Title: Pharmacovigilance Associate

About the Role
Are you a graduate with a background in life sciences or a healthcare-related field? The PV Associate role offers a fantastic opportunity to kickstart your career in drug safety. You’ll be part of a project team performing pharmacovigilance activities for a diverse range of clinical trial and post-marketing projects.

We are looking for proactive, enthusiastic individuals ready to grow and contribute to patient safety.


Responsibilities

  • Process Individual Case Safety Reports (ICSRs) from various sources (post-marketing and clinical trials) in compliance with regulations, client requirements, and internal procedures.
  • Perform tasks like triage, data entry, quality review, and submissions.
  • Conduct reconciliation activities for received reports.
  • Work under the supervision and mentorship of experienced colleagues.

Qualifications

  • Language Skills: Advanced English and German proficiency (verbal and written), at least B2 level.
  • Educational Background: Degree in life sciences, biomedicine, or healthcare-related fields (e.g., chemistry, biology, biotechnology, veterinary science).
  • No prior experience required – ideal for recent graduates!
  • Eager to learn and committed to ensuring patient safety.
  • Strong multitasking, time management, and organizational skills.
  • Excellent interpersonal and communication abilities.

What We Offer

  • Competitive salary.
  • A dynamic team environment in a rapidly growing company, enabling quick career growth.
  • A multicultural workplace with English as the primary company language.
  • Emphasis on personal and professional growth.
  • Extensive pharmacovigilance training conducted by seasoned professionals, including international seminars.
  • A friendly, supportive work environment with regular social events.

Our Core Values
At PrimeVigilance, our values guide everything we do. If these resonate with you, we’d love to have you on our team:

  • Quality
  • Integrity & Trust
  • Drive & Passion
  • Agility & Responsiveness
  • Belonging
  • Collaborative Partnerships

We look forward to your application. Let’s work together to make a positive impact on patient safety!