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Pv Associate - German Speaker

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

Company Overview

PrimeVigilance, part of Ergomed Group, is a specialized mid-size pharmacovigilance service provider founded in 2008. We’ve consistently achieved organic growth and have a global team across Europe, North America, and Asia, offering services in Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance. We provide exceptional support to pharmaceutical and biotechnology companies, maintaining long-term relationships and becoming a leader in our field. Our team covers all therapy areas, including medical devices.

At PrimeVigilance, we invest in our staff’s growth through excellent training and development opportunities. We prioritize employee well-being, mental health, and work-life balance, ensuring a supportive environment where high-quality client service can thrive.

Job Overview

We are looking for a Pharmacovigilance (PV) Associate with a Life Sciences or biomedical background (e.g., chemistry, biology, biotechnology, veterinary science). This is a fantastic opportunity for new graduates to launch their careers in drug safety. As a PV Associate, you will support a variety of pharmacovigilance activities as part of a project team for PrimeVigilance. You will work on both clinical trials and post-marketing teams, performing tasks such as case processing and reconciliation, all while learning from more experienced colleagues.

Key Responsibilities

  • Process Individual Case Safety Reports (ICSRs) from post-marketing and clinical trial sources, ensuring compliance with regulations, PrimeVigilance procedures, and client requirements.
  • Focus on triage, data entry, quality review, and submission workflow for ICSRs.
  • Assist with reconciliation activities for received reports.
  • Work under supervision and mentorship to develop your skills in pharmacovigilance.

Qualifications

  • Advanced English and German language skills (minimum B2 level).
  • A degree in Life Sciences or Biomedical Sciences (e.g., chemistry, biology, biotechnology, veterinary science).
  • Strong interest in learning and contributing to patient safety.
  • Excellent organizational, multitasking, and issue management skills with great attention to detail.
  • Strong interpersonal and communication skills.

Why Join PrimeVigilance?

At PrimeVigilance, we prioritize diversity, equity, and inclusion, fostering an environment where all backgrounds are valued and can thrive. We believe that collaboration and a human-first approach are key to our success and the well-being of our employees.

We offer:

  • Competitive salary.
  • Opportunities for fast career growth in a dynamic and multicultural environment.
  • Extensive training in pharmacovigilance, both internal and at prestigious seminars abroad.
  • A friendly, supportive work culture with regular social events.
  • English as the company language.

If our core values of Quality, Integrity, Trust, Drive, Passion, and Collaboration resonate with you, we would love to welcome you to our team.