Remote Clinical Trial Coordinator opportunity – Thermo Fisher Scientific
- Clinical Trial Coordinator Vacancy for Graduates | Remote India
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Summary Table
- FAQs
- 1. Who can apply for the Clinical Trial Coordinator role?
- 2. Is this a fully remote opportunity?
- 3. What skills are important for this role?
- 4. What does a Clinical Trial Coordinator do?
- 5. How do I apply?
Clinical Trial Coordinator Vacancy for Graduates | Remote India
Apply for the Clinical Trial Coordinator role at Thermo Fisher Scientific. Openings for graduates with 2+ years experience. Fully remote across India.
Thermo Fisher Scientific is inviting experienced clinical research professionals to apply for the Clinical Trial Coordinator position. This remote role is ideal for candidates who want to contribute to high‑impact global clinical trials while working with one of the most trusted names in life sciences. The position supports end‑to‑end trial operations and plays a key role in ensuring accuracy, compliance, and operational efficiency across studies.
Company Overview
Thermo Fisher Scientific is a global leader in scientific innovation, clinical research services, and drug development support. Through its PPD® clinical research portfolio, the company helps clients accelerate the development of new therapies and improve patient outcomes. With operations in more than 100 countries, Thermo Fisher provides integrated clinical trial solutions backed by robust scientific expertise and state‑of‑the‑art technology.
Job Role & Responsibilities
The Clinical Trial Coordinator (CTC) provides operational, administrative, and technical support to project teams throughout the lifecycle of a clinical trial. Core responsibilities include:
- Support audit readiness by ensuring proper review and maintenance of essential documents.
- Assist with site activation activities and ensure timely progress across all startup milestones.
- Contribute to feasibility assessments and support the investigator/site identification process.
- Build collaborative relationships with site personnel and local teams.
- Maintain study documentation according to ICH‑GCP, regulatory requirements, and sponsor guidelines.
- Support data accuracy by analyzing project‑specific systems, trackers, and logs.
- Coordinate with study teams during monitoring visits, site communication, and study updates.
- Assist new team members during the onboarding phase as a buddy.
- Participate in process improvements and departmental initiatives.
- Provide seamless administrative support throughout study execution and closeout.
Eligibility / Qualifications
Candidates should meet the following criteria:
- Bachelor’s degree preferred (Life Sciences, Pharmacy, Biotechnology, Nursing, or related fields).
- Minimum of 2 years of experience in clinical research or a similar role.
- Strong organizational skills and ability to manage multiple tasks under tight timelines.
- Solid knowledge of ICH‑GCP, country‑specific regulations, and clinical operations processes.
- Proficiency in MS Office tools and ability to learn clinical trial databases and systems.
- Strong communication and interpersonal skills.
- Ability to work independently and collaboratively within cross‑functional teams.
- Flexibility and adaptability to changing study demands.
Location & Salary
- Work Mode: Fully Remote (India)
- Work Schedule: Monday to Friday
- Salary details are as per company standards and will be discussed with shortlisted candidates.
Application Process
Interested candidates can apply directly through the official Thermo Fisher Scientific career portal:
Apply here: https://jobs.thermofisher.com/global/en/job/R-01329479/Clinical-Trial-Coordinator
Summary Table
| Category | Details |
|---|---|
| Company | Thermo Fisher Scientific |
| Vacancies | Not Disclosed |
| Required Education | Bachelor’s degree (Life Sciences, Pharmacy, Biotechnology, Nursing, related fields) |
| Experience | Minimum 2 years |
| Location | Remote – India |
FAQs
1. Who can apply for the Clinical Trial Coordinator role?
Candidates with at least 2 years of clinical research experience and a bachelor’s degree in a science or healthcare discipline are eligible.
2. Is this a fully remote opportunity?
Yes, this position is fully remote within India.
3. What skills are important for this role?
Strong organization, knowledge of ICH‑GCP, communication skills, multitasking ability, and proficiency in MS Office tools.
4. What does a Clinical Trial Coordinator do?
A CTC supports site activation, documentation, compliance, feasibility, communication with sites, and overall project coordination across study phases.
5. How do I apply?
Submit your application through the official link provided above.
To apply for this job please visit jobs.thermofisher.com.
