Instagram
youtube
Facebook

Medical Contact Center Associate Ii

1-6 years
Not Disclosed
10 Nov. 25, 2025
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

Medical Contact Center Associate II

Category: Clinical
Job ID: 255006
Locations: Multiple (Available in 3 Locations)
Employment Type: Full-Time

Job Overview

The Medical Contact Center Associate II is responsible for managing medical information inquiries, product quality complaints, and general queries received through phone calls, emails, and other communication channels. This role supports drug safety operations and ensures compliance with global regulatory standards. Proficiency in French communication is essential, along with the ability to work in 24x7 rotational shifts.

This position is suitable for professionals with pharmacovigilance, medical information, or call-center experience within the pharmaceutical, biotechnology, or CRO sectors.


Key Responsibilities

  • Respond to medical information queries, product quality complaints, and general questions received through phone, email, fax, and other channels (French communication required).

  • Receive, document, and report Adverse Drug Reactions (ADRs) within regulatory timelines and as per internal SOPs and work instructions.

  • Execute drug safety data management tasks including call intake, case documentation, peer review, and case follow-up.

  • Support multiple operational activities such as information tracking, quality checks, metrics monitoring, training coordination, and data reconciliation.

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

  • Conduct training sessions and assess training effectiveness for team members.

  • Ensure high-quality, accurate processing of safety and medical information data.

  • Perform additional duties as assigned by the management team.


Qualifications (Minimum Requirements)

  • Proficiency in French (spoken and written).

  • Strong command of English, both written and verbal.

  • Educational pathways include:

    • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Medical Sciences, or related fields + 2–3 years of safety experience

    • BS/BA degree + 2–3 years of safety experience

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

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

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

  • Safety experience includes hands-on involvement with AE/SAE processing, narrative generation, safety databases, regulatory submissions, and case processing.

  • Relevant experience includes roles in Medical Affairs, Clinical Data Entry, Data Management, Clinical Monitoring, Regulatory Affairs, or Quality Assurance.


Experience Required

  • Minimum 2–3 years of pharmacovigilance or drug safety experience, depending on educational background.

  • Experience working in call center operations is preferred.

  • Background in pharmaceutical, biotech, or CRO environments is desirable.


Preferred Qualifications

  • Degree in Biological Sciences, Pharmacy, Nursing, Life Sciences, Chemistry, or related disciplines.

  • Strong written and verbal communication skills.

  • Ability to manage inbound and outbound medical calls professionally.

  • Capability to analyze and synthesize medical and safety information.

  • Knowledge of regulatory requirements, pharmacovigilance principles, and ICH GCP guidelines.

  • Proficiency in Microsoft Office applications with strong attention to detail.

  • Ability to work independently with moderate supervision while functioning effectively as part of a team.