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Medical Contact Center Associate Ii (French Speaker)

2-4 years
Not Disclosed
10 Oct. 19, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Medical Contact Center Associate II (French Speaker)

📍 Available in 3 Locations
Category: Clinical
Job ID: 254713


Job Summary

The Medical Contact Center Associate II (French Speaker) is responsible for managing medical information inquiries, product quality complaints, and adverse event reporting in both French and English. This role combines pharmacovigilance, medical communication, and data management in a fast-paced, compliant environment.

The ideal candidate will be fluent in French, experienced in call center operations or drug safety, and possess strong analytical and communication skills.


Key Responsibilities

Medical Information Handling

  • Respond to medical information queries, product quality complaints, and general inquiries received via telephone, email, or fax (primarily in French).

  • Accurately record and process all received information following internal procedures and regulatory requirements.

Adverse Event Reporting

  • Receive, document, and report Adverse Drug Reactions (ADRs) within required timelines as per regulations and company SOPs/WIs.

  • Ensure accuracy and compliance in safety data entry and narrative preparation.

Data Management & Quality Control

  • Execute drug safety data management processes, including:

    • Call intake and dialogue documentation

    • Peer review and case follow-up

  • Perform tracking and reconciliation of information from multiple data sources.

  • Support ongoing quality control (QC) and process improvement initiatives.

Training & Process Support

  • Develop and update training materials based on procedural, system, and regulatory changes.

  • Conduct and evaluate training sessions for new and existing staff.

  • Take responsibility for the accuracy and quality of processed data.

Other Duties

  • Perform additional tasks as assigned by management to support department goals and operational efficiency.


Qualifications

Education (Minimum Required)

  • Bachelor’s or Master’s degree in Pharmacy, Life Science, or Medical Science

    • BS/BA: 2–3 years of safety experience

    • MA/MS/PharmD: 1–2 years of safety experience

    • Associate degree: 4–5 years relevant experience (or 2+ years safety experience)

    • Non-degree: 5–6 years relevant experience (or 2+ years safety experience)

Fortrea may consider relevant and equivalent experience in lieu of educational requirements.


Experience

Minimum Required

  • 2–3 years of pharmacovigilance/safety experience, including:

    • Adverse event (AE/SAE) case processing

    • Narrative writing

    • Query management

    • Experience with safety databases and regulatory submissions

Relevant Experience Includes

  • Work in pharmaceutical, biotechnology, or CRO industries within:

    • Medical Affairs

    • Clinical Data Management/Monitoring

    • Regulatory Affairs

    • Quality Assurance

Preferred

  • Call center operations experience

  • 24x7 rotational shift flexibility

  • Fluent French (C-level proficiency, verbal and written)

  • Degree in Biological Sciences, Pharmacy, Nursing, Life Sciences, or Chemistry


Skills & Competencies

  • Excellent French and English communication skills (written & verbal)

  • Strong analytical ability to interpret medical information accurately

  • Understanding of regulatory requirements, Good Pharmacovigilance Practices (GVP), and ICH-GCP guidelines

  • Technical proficiency in Microsoft Office applications

  • Exceptional attention to detail and accuracy

  • Team-oriented, proactive, and capable of working independently with moderate supervision


Work Environment

  • 💻 Remote / Home-based position

  • Requires flexibility for 24x7 rotational shifts


Additional Information

  • Learn more about EEO & Accommodation requests here (link placeholder)

  • Employer: Fortrea — advancing global clinical research and patient safety through excellence in pharmacovigilance and compliance.