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Cra (Level Ii)

Thermo Fisher Scientific
Thermo Fisher Scientific
0-2 years
Not Disclosed
10 Dec. 31, 2025
Job Description
Job Type: Full Time 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

Job Title: Clinical Research Associate (CRA) – Level II

Job ID: R-01331413
Location: Remote, India (Metro city base required)
Job Type: Full-time
Work Mode: Fully Remote
Category: Clinical Research
Experience Required: Minimum 3 years (On-site Monitoring)


Company Overview

Thermo Fisher Scientific is a global leader in scientific services, enabling customers to make the world healthier, cleaner, and safer. Through its PPD® clinical research portfolio, Thermo Fisher supports the development of innovative therapies by delivering high-quality clinical research services to pharmaceutical, biotechnology, and medical device companies worldwide.

The Clinical Research Services team plays a critical role in accelerating drug development and bringing life-saving treatments to market by combining deep scientific expertise with operational excellence.


Role Overview

The Clinical Research Associate (CRA) – Level II will independently manage and monitor clinical trial sites to ensure protocol compliance, data integrity, and adherence to regulatory and ethical standards. This role is ideal for experienced CRAs who are confident in site management, regulatory compliance, and cross-functional collaboration in a remote working environment.


Key Responsibilities

  • Independently coordinate and monitor all aspects of assigned clinical trials to ensure data accuracy, subject safety, and regulatory compliance.

  • Conduct on-site and remote monitoring activities in accordance with ICH-GCP, SOPs, and regulatory requirements.

  • Collaborate with cross-functional teams including Clinical Operations, Data Management, and Regulatory Affairs to ensure successful study execution.

  • Track study progress and ensure timely completion of monitoring visits, reports, and action items.

  • Maintain accurate, complete, and audit-ready documentation in Trial Master File (TMF) and other systems.

  • Ensure strict adherence to company policies, study protocols, and industry standards for flawless trial execution.


Required Qualifications & Skills

  • Minimum 3 years of experience as a Clinical Research Associate, with proven expertise in on-site monitoring.

  • Strong knowledge of Indian regulatory requirements, ICH-GCP, and clinical trial conduct.

  • Excellent organizational and time management skills with the ability to handle multiple studies simultaneously.

  • Ability to prioritize tasks and meet tight deadlines in a fast-paced clinical research environment.

  • Strong written and verbal communication skills for effective collaboration with investigators and internal teams.

  • Self-motivated, detail-oriented, and committed to high-quality clinical research delivery.


Location Requirement

  • Candidates must be based in or willing to be based in a major metro city in India, including:

    • Mumbai

    • Delhi NCR

    • Bengaluru

    • Hyderabad

    • Ahmedabad


Why Join Thermo Fisher Scientific

  • Work with a globally recognized CRO at the forefront of clinical research innovation.

  • Contribute to clinical trials that address some of the world’s most critical health challenges.

  • Thrive in a collaborative, inclusive, and performance-driven work culture.

  • Gain exposure to global studies and career advancement opportunities within clinical operations.

  • Enjoy the flexibility of a fully remote role with strong organizational support.


How to Apply

Apply through The Pharma Daily to take the next step in your clinical research career and join a global organization committed to advancing science and improving patient lives.