Full-Time
Salary: 25k to 30k
Positions: 10

Pharmacovigilance Services Associate

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Job Description

 Location: Remote – India
Job ID: R-01326248
Category: Clinical Research
Employment Type: Full-time
Work Schedule: Standard (Mon–Fri)
Work Model: Fully Remote / Onsite
Company: Thermo Fisher Scientific (PPD® Clinical Research Services)

About the Role

At Thermo Fisher Scientific, every role contributes to our mission of making the world healthier, cleaner, and safer. As a Clinical Research Associate (CRA) at PPD® Clinical Research Services, you will play a key role in ensuring the quality, accuracy, and integrity of clinical trials conducted globally.

You’ll be part of a high-performing team of clinical professionals who bring expertise and innovation to every stage of the research process — from study start-up to closeout — ensuring that investigational therapies reach patients faster and more safely.

This is an opportunity to make a global impact while developing your career within one of the world’s most respected scientific organizations.

Role & Responsibilities

  • s are complete and audit-ready.

  • Assess investigational product (IP) accountability through inventory and records review.

  • Prepare monitoring reports, documentation, and correspondence in compliance with business writing standards and project timelines.

  • Collaborate with internal teams to track project progress, support investigator payments, and ensure accurate system updates in CTMS.

  • Identify potential investigators and participate in investigator meetings as needed.

Educational Qualification

Education:

  • Bachelor’s degree in Life Sciences or a related discipline.

  • Registered Nursing certification or equivalent qualification may also be considered.

Experience:

  • Minimum 2+ years of on-site clinical monitoring experience in a pharmaceutical, biotechnology, or CRO setting.

  • Demonstrated understanding of ICH-GCP guidelines and clinical trial regulations.

Location

Remote – India

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