Thermo Fisher Scientific Hiring CRA (Level I, II & Sr CRA) & Clinical Trial Coordinator II | Remote / Onsite

✔ Verified by Medical Jobs India

CRA (Level I, II & Sr CRA) & Clinical Trial Coordinator II

Thermo Fisher Scientific (PPD®)

Remote / Onsite

2–4+ Years

Clinical Research

CRA / CTC

Full-Time

📄 About the Company

Thermo Fisher Scientific, through its PPD® Clinical Research Services, is a global leader in clinical research, laboratory services, and life sciences solutions.

The organization supports global clinical trials across multiple therapeutic areas while maintaining the highest standards of ICH-GCP, regulatory compliance, and patient safety.

📌 Job Overview

Thermo Fisher Scientific is hiring for multiple clinical research roles including Clinical Research Associate (CRA I, CRA II, Sr. CRA) and Senior Clinical Trial Coordinator / Clinical Trial Coordinator II.

These roles offer the opportunity to work on global clinical trials, collaborate with international project teams, and contribute to life-changing therapies.

📌 Job 1 – Clinical Research Associate (CRA I / CRA II / Sr. CRA)

Location: Remote / Onsite (India)

Experience: Minimum 2+ Years (Level based)

Work Schedule: Standard (Monday–Friday)

Employment Type: Full-Time

Monitor investigator sites using risk-based monitoring (RBM)
Ensure compliance with protocol, ICH-GCP, SOPs, and regulations
Conduct site initiation, monitoring, and close-out visits
Perform SDV, SDR, and CRF reviews for data accuracy
Maintain essential documents and audit readiness
Communicate with sites, sponsors, and project teams
Prepare monitoring reports, follow-up letters, and status updates

Eligibility:

Bachelor’s degree in Life Sciences or Registered Nursing
2+ years of experience as a Clinical Research Monitor
Strong knowledge of ICH-GCP and clinical trial regulations
Proficiency in MS Office and CTMS tools

📌 Job 2 – Senior Clinical Trial Coordinator / Clinical Trial Coordinator II

Location: Remote (India)

Experience: 4+ Years

Work Schedule: Second Shift (Afternoons)

Employment Type: Full-Time

Provide administrative and technical support to global project teams
Maintain study documents, trackers, and trial systems
Work with Veeva Vault, eTMF, and CTMS platforms
Support regulatory document review and submissions
Assist with site files, pharmacy binders, and translation QC
Organize project meetings and prepare meeting minutes
Support RBM activities and global project managers

Eligibility:

Bachelor’s degree preferred
4+ years experience as a Clinical Trial Coordinator
Hands-on experience with global clinical trials
Strong organizational, multitasking, and communication skills

💼 Why Join Thermo Fisher Scientific?

Work on global, high-impact clinical trials
Career growth in a world-leading CRO environment
Flexible, collaborative, and supportive workplace
Exposure to digital and decentralized trial models
Strong learning and professional development culture

📌 Note Before You Apply:
Please select the appropriate role from the dropdown below. Carefully review the eligibility and experience requirements before applying to increase your chances of shortlisting.

🔎 For More Medical Jobs