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Medical Contact Center Associate Ii

Fortrea
Fortrea
2-4 years
Not Disclosed
Bangalore, Mumbai, Pune, India
10 March 24, 2026
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 – Pharmacovigilance

Location: Multiple Locations
Job Type: Full-Time
Category: Clinical / Pharmacovigilance
Experience Required: 2–4 Years
Job ID: 261040

Overview
A dynamic opportunity is available for a Medical Contact Center Associate II specializing in pharmacovigilance and medical information services. This role is designed for professionals fluent in French and English, responsible for handling medical inquiries, product quality complaints, and adverse drug reaction reporting while ensuring compliance with global regulatory standards.

Key Responsibilities
You will manage inbound and outbound medical information requests received via telephone, email, and other communication channels, primarily in French. The role involves accurate documentation, evaluation, and reporting of adverse drug reactions in accordance with regulatory timelines and internal standard operating procedures.

You will execute pharmacovigilance processes, including call intake, documentation of call dialogues, case processing, peer review, and follow-up activities. Additionally, you will support quality control processes, data reconciliation, and tracking of safety metrics to ensure data integrity and compliance.

The position also requires developing and updating training materials based on evolving regulatory requirements and internal processes. You may be involved in delivering training sessions and evaluating their effectiveness. Maintaining high standards of data quality and contributing to continuous process improvement initiatives are essential aspects of the role.

Educational Qualifications
Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Medical Sciences, or a related field. PharmD candidates are also eligible.

Experience Requirements
2 to 4 years of experience in pharmacovigilance, drug safety, or related clinical domains. Candidates with relevant experience in medical information, clinical data management, regulatory affairs, or quality assurance may also be considered.

Required Skills and Competencies
Fluency in French and English (both written and spoken)
Strong understanding of pharmacovigilance processes and adverse event reporting
Ability to manage inbound and outbound medical communication effectively
Good knowledge of global regulatory requirements and ICH-GCP guidelines
Strong analytical and data interpretation skills
High attention to detail and commitment to data quality
Proficiency in Microsoft Office tools
Ability to work independently as well as in a team-oriented environment
Willingness to work in rotational shifts (24x7 support model)

Preferred Qualifications
Experience in call center or medical information contact center operations
Background in biological sciences, pharmacy, nursing, or chemistry
Experience with safety databases and case processing workflows

Why Join
This role offers an excellent opportunity to build a specialized career at the intersection of medical information services and pharmacovigilance. You will gain exposure to global safety reporting systems, multilingual communication, and regulatory compliance while contributing to patient safety and high-quality healthcare support services.