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Pharmacovigilance Reporting Associate (French/German Language)

0-2 years
Not Disclosed
10 Oct. 2, 2024
Job Description
Job Type: Remote 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

Pharmacovigilance Reporting Associate (French/German Language)

Company Overview:
ICON plc is a leading healthcare intelligence and clinical research organization. We take pride in fostering an inclusive environment that drives innovation and excellence. We invite you to join us in our mission to shape the future of clinical development.

Role Overview:
The Pharmacovigilance (PV) Reporting Associate acts as a processor of safety reporting intelligence and may lead standalone safety reporting projects, providing management support as needed. This position focuses on safety reporting activities, requiring a customer-oriented approach and a mindset prepared for audits and inspections. The role primarily involves Medical Information tasks, which include communicating with the public and healthcare professionals.

Key Responsibilities:

  • Review and process safety events (pre-marketing, post-marketing, medical device, and drug-related) following assigned tasks and project-specific procedures.
  • Conduct adverse event follow-ups through written communication and phone calls based on client requirements.
  • Review abstracts and full articles to identify safety information from literature sources for both pre and post-marketed products.
  • Generate data listings from the safety database, ensuring data accuracy.
  • Provide input on and review safety tracking systems for quality and accuracy while assisting in maintaining project files.
  • Perform safety reviews of clinical and diagnostic data as part of case processing.
  • Develop and ensure the effective execution of the Safety Management Plan, including specific processes to maintain consistency within projects.
  • Assist with post-marketing safety activities such as PSMF, RMP, and PBRER.
  • Support the Qualified Person for Pharmacovigilance as needed.
  • Liaise with investigational sites, reporters, and sponsors regarding safety issues.
  • Collaborate with ICON Medical Monitors, project managers, and other departments as appropriate.

Requirements:

  • Background or education in healthcare (Nursing, Pharmacy, Medicine).
  • Fluency in English and either German or French.
  • Strong communication skills.

What ICON Offers You:
Our success is built on the quality of our people, which is why we prioritize creating a diverse culture that rewards high performance and nurtures talent.

In addition to a competitive salary, ICON provides a range of benefits designed to promote well-being and work-life balance for you and your family, including:

  • Various annual leave entitlements.
  • Health insurance options tailored to your and your family's needs.
  • Competitive retirement planning offerings.
  • Global Employee Assistance Programme (LifeWorks), providing 24-hour access to a network of over 80,000 professionals to support your well-being.
  • Life assurance.
  • Flexible country-specific benefits, such as childcare vouchers, bike purchase schemes, discounted gym memberships, and health assessments.

Visit our careers site to learn more about the benefits ICON offers.

Commitment to Diversity:
ICON is an equal opportunity and inclusive employer, dedicated to providing a workplace free from discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

If you require a reasonable accommodation during the application process or to perform essential job functions due to a medical condition or disability, please let us know or submit a request here.

Interested in the Role?
If you’re unsure whether you meet all the requirements, we encourage you to apply anyway—there’s a good chance you’re exactly what we’re looking for at ICON, whether for this position or others.

Current ICON Employees:
If you are a current employee at ICON, please click here to apply.