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Cra (Level Ii)

Thermo Fisher Scientific
Thermo Fisher Scientific
3 years
preferred by company
10 Jan. 9, 2026
Job Description
Job Type: Full Time Remote 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

Clinical Research Associate (CRA) Level II – Remote, India

Location: Remote, India (Candidates should be based in major metro cities: Mumbai, Delhi NCR, Bengaluru, Hyderabad, Ahmedabad)
Job ID: R-01331413
Job Type: Full-Time
Category: Clinical Research / Monitoring
Work Mode: Fully Remote

About Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in scientific research, providing innovative solutions that advance healthcare and improve patient outcomes worldwide. Our Clinical Research team, powering the PPD® clinical research portfolio, operates at the forefront of drug development, supporting clinical trials across multiple therapeutic areas and regions.

We foster a dynamic and inclusive work environment, where collaboration, innovation, and excellence are key to achieving meaningful results.

Role Overview

We are seeking an experienced Clinical Research Associate (CRA) Level II to coordinate and monitor clinical trials in India. This role offers the opportunity to work on high-impact projects, ensuring compliance with regulatory guidelines and Good Clinical Practice (GCP). You will be responsible for site management, data integrity, and regulatory adherence, contributing to the successful execution of clinical studies.

Key Responsibilities

  • Lead and coordinate all aspects of clinical trial monitoring to ensure data quality, regulatory compliance, and patient safety.

  • Conduct on-site and remote visits to investigative sites, applying risk-based monitoring principles.

  • Collaborate with cross-functional teams to implement study protocols and achieve project milestones.

  • Monitor study progress, identify risks, and provide timely reporting to project management.

  • Ensure accurate and complete documentation of all clinical activities in accordance with GCP and company SOPs.

  • Identify, escalate, and resolve site-related issues, ensuring continuous compliance with protocol and regulatory requirements.

  • Participate in investigator meetings, site initiation, and study close-out activities.

Qualifications & Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field.

  • Minimum 3 years of on-site clinical research monitoring experience in India.

  • Strong knowledge of Indian regulatory requirements and international GCP standards.

  • Experience working with multiple study protocols, sponsors, and CRO environments.

Skills & Competencies

  • Exceptional organizational and time management skills to handle multiple projects simultaneously.

  • Strong analytical, problem-solving, and decision-making abilities.

  • Excellent written and verbal communication skills in English; ability to collaborate with diverse teams.

  • Attention to detail and commitment to high-quality documentation and compliance.

  • Ability to work independently and proactively, while maintaining a team-oriented mindset.

  • Motivated to contribute to clinical research excellence and patient-centric outcomes.

Why Join Us

  • Global Exposure: Work on clinical trials across therapeutic areas and collaborate with international teams.

  • Career Growth: Access mentorship, training programs, and opportunities to advance in Clinical Operations.

  • Impactful Work: Contribute to the development of life-changing therapies and ensure high-quality clinical research outcomes.

  • Collaborative Environment: Join a culture of innovation, integrity, and shared success.

Thermo Fisher Scientific is committed to enabling our teams to achieve their potential while advancing science to improve global health.

Thermo Fisher Scientific is an Equal Employment Opportunity Employer.