Work-from-Home Clinical Trial Coordinator vacancies Thermo Fisher Scientific
- Clinical Trial Coordinator Jobs | Remote India
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Work Setup
- Salary & Benefits
- Application Process
- Why Join Thermo Fisher Scientific?
- FAQs
- Vertical Summary Table
Clinical Trial Coordinator Jobs | Remote India
Apply for Sr. Clinical Trial Coordinator jobs in India (Remote). Bachelor’s degree required with 4+ years experience in clinical research.
Pharma professionals seeking rewarding Clinical Trial Coordinator jobs in India can now apply for an exciting full-time remote opportunity with Thermo Fisher Scientific (PPD Division) — a global leader in clinical research and contract research services (CRO). This role offers a chance to contribute to breakthrough healthcare innovations, working with cutting-edge tools and a collaborative global team.
Company Overview
Thermo Fisher Scientific, through its PPD® Clinical Research Services, stands at the forefront of global drug development and clinical trial management. The company partners with leading pharmaceutical, biotech, and healthcare organizations to bring new therapies to market faster. With a strong focus on scientific innovation and patient safety, Thermo Fisher empowers professionals to advance their careers while making a tangible difference in global healthcare.
Job Role & Responsibilities
As a Clinical Trial Coordinator (or Sr. Coordinator), you will provide essential administrative and technical support to ensure smooth clinical operations across global studies. This role demands precision, teamwork, and adaptability to support both local and global clinical trial activities.
Key Responsibilities:
- Coordinate and facilitate project activities per assigned study tasks and timelines.
- Maintain study-specific documentation and ensure (e)TMF compliance.
- Manage system access and study team lists for cross-functional teams.
- Provide support in eTMF, Veeva Vault, GoBalto, and CTMS tools.
- Oversee country and investigator file reviews and maintain quality documentation.
- Prepare and distribute Investigator Site Files (ISF), Pharmacy binders, and non-clinical supplies.
- Assist in study material translation and QC processes.
- Support risk-based monitoring (RBM) and regulatory documentation tracking.
- Organize client/internal meetings, prepare meeting minutes, and track project progress.
- Ensure timely submission and tracking of regulatory and IRB/IEC documents.
- Collaborate with global Project Managers and clinical teams to ensure timely delivery of milestones.
Eligibility / Qualifications
- Education: Bachelor’s Degree in Life Sciences, Pharmacy, Biotechnology, or related field (e.g., B.Pharm, M.Sc Clinical Research, B.Sc Nursing, B.Tech Biotech).
- Experience: Minimum 4+ years of experience as a Clinical Trial Coordinator or related role in global clinical research.
- Technical Skills: Proficiency in Veeva Vault, CTMS, eTMF systems, and MS Office suite.
- Soft Skills: Strong attention to detail, analytical thinking, and organizational skills.
- Regulatory Knowledge: Understanding of ICH-GCP, country-specific regulations, SOPs, and study documentation standards.
- Communication: Excellent verbal and written English proficiency; local language fluency preferred.
Location & Work Setup
- Location: Fully Remote (India)
- Work Schedule: Second Shift (Afternoon)
- Environment: Office-based setup (remote operations)
Salary & Benefits
Competitive salary package based on experience and qualifications.
Benefits include flexible work arrangements, professional development programs, and access to world-class clinical tools and systems.
Application Process
Interested candidates can apply directly through Thermo Fisher Scientific’s official portal:
Apply Here
Apply before positions fill! Secure your opportunity to work with one of the most trusted names in global clinical research.
Why Join Thermo Fisher Scientific?
- Be part of a global leader in pharmaceutical and biotechnology research.
- Work with innovative digital systems and tools like eTMF, CTMS, and Veeva Vault.
- Collaborate with top professionals in Clinical Research, Data Management, and Regulatory Affairs.
- Access professional growth and continuous learning opportunities.
- Contribute to developing life-saving drugs and global healthcare advancements.
FAQs
Q1: Who can apply for this Clinical Trial Coordinator role?
Candidates with a Bachelor’s degree in life sciences or pharmacy and 4+ years of experience in clinical trial coordination are eligible.
Q2: Is this a remote position?
Yes, this role is fully remote and open to applicants across India.
Q3: What tools or systems should I be familiar with?
Veeva Vault, eTMF, CTMS, and GoBalto are key systems used in this role.
Q4: What shift is required for this position?
The job follows a second (afternoon) shift schedule.
Q5: How can I apply?
Visit the official Thermo Fisher career page to submit your application.
Vertical Summary Table
| Company | Thermo Fisher Scientific (PPD Division) |
|---|---|
| Vacancies | Sr. Clinical Trial Coordinator / Clinical Trial Coordinator II |
| Required Education | Bachelor’s in Life Sciences, Pharmacy, Biotechnology, Nursing, Clinical Research |
| Experience | Minimum 4+ years in Clinical Research Coordination |
To apply for this job please visit jobs.thermofisher.com.
