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Junior Micc Associate

Navitas Life Sciences
Navitas Life Sciences
1-3 years
Not Disclosed
Princeton Junction, United States
10 March 27, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Junior MICC Associate | Pharmacovigilance & Medical Information Jobs

Company: Not Disclosed
Location: India
Job Type: Full-Time
Work Mode: On-site / Hybrid (as per company policy)
Experience: 1–3 Years
Category: Pharmacovigilance / Medical Information / Drug Safety


Job Overview

We are hiring a Junior MICC Associate (Medical Information Contact Center) to support pharmacovigilance operations, adverse event (AE) intake, and medical information services.

This role is crucial in handling safety case intake, product quality complaints (PQC), medical inquiries (MI), and general inquiries (GI) while ensuring compliance with global pharmacovigilance guidelines and regulatory standards.

You will act as a frontline interface for drug safety communication, ensuring accurate documentation, follow-ups, and high-quality case processing in a regulated environment.


Key Responsibilities

Case Intake & Pharmacovigilance Operations

  • Handle incoming calls and emails related to AE, PQC, MI, and GI

  • Perform case intake, duplicate checks, and case registration

  • Ensure accurate and complete documentation of safety cases

Follow-Up & Communication

  • Conduct follow-up inquiries via phone and email for case completeness

  • Communicate effectively with healthcare professionals, patients, and clients

  • Translate inquiries when required to ensure accurate understanding

Medical Information Support

  • Assist in handling medical information queries (MI)

  • Support documentation and response preparation aligned with medical and regulatory standards

Documentation & Compliance

  • Develop and maintain MICC-related documentation and records

  • Ensure compliance with GVP, ICH guidelines, and pharmacovigilance processes

  • Maintain proper tracking and reporting of cases


Required Skills & Qualifications

Education

  • Graduate/Postgraduate in Life Sciences, Pharmacy, Dentistry, or Allied Health Sciences

Experience

  • 1–3 years of experience in MICC / pharmacovigilance / medical information roles

Technical Skills

  • Understanding of:

    • Adverse Event (AE) reporting and pharmacovigilance processes

    • Medical Information (MI) handling and case processing

    • Product Quality Complaints (PQC)

  • Familiarity with safety databases and PV workflows (preferred)

Core Competencies

  • Strong verbal and written communication skills

  • Attention to detail and accuracy in case documentation

  • Ability to handle client communication and coordination

  • Multitasking ability in a fast-paced environment

  • Problem-solving mindset and adaptability


Preferred Skills

  • Experience with global pharmacovigilance processes

  • Exposure to ICSR case processing and safety databases (Argus, ArisG, etc.)

  • Knowledge of GVP and ICH pharmacovigilance guidelines

  • Multilingual skills for handling global inquiries


Perks & Benefits

  • Opportunity to work in pharmacovigilance and drug safety operations

  • Exposure to global medical information and safety case handling

  • Career growth in PV, medical writing, and regulatory affairs

  • Dynamic and collaborative work environment

  • Hands-on experience with real-world drug safety data


Compensation

  • Salary Range: Not disclosed (competitive as per PV industry standards)


About the Company

A growing pharmacovigilance and healthcare solutions organization focused on delivering medical information services, drug safety monitoring, and regulatory compliance support to global pharmaceutical clients.


Call to Action

If you want to start or grow your career in pharmacovigilance, medical information, and drug safety, this role is your entry point into a high-demand domain.

Be part of a system that directly contributes to patient safety and global healthcare outcomes.

👉 Apply now and step into the world of pharmacovigilance! 🚀