Thermo Fisher Scientific Jobs in Mumbai: Clinical Trial Coordinator – FSP
Thermo Fisher Scientific is hiring for the position of Clinical Trial Coordinator – FSP in Mumbai, Maharashtra, India. This is a full-time, fully remote opportunity for candidates with at least 2 years of experience in global clinical trial support as a Clinical Trial Coordinator or Project Coordinator. Candidates with experience in Phase II and III clinical studies, Veeva Vault, and the electronic Trial Master File (eTMF) lifecycle may find this opportunity relevant.
Company Overview
Thermo Fisher Scientific provides scientific services and solutions that support pharmaceutical research, clinical development, and healthcare innovation. Its PPD clinical research business supports clinical trials for pharmaceutical and biotechnology companies worldwide.
The Clinical Trial Coordinator – FSP position involves providing administrative and technical support to clinical study teams, maintaining study documentation, supporting site activation, and contributing to regulatory inspection readiness.
Job Details
| Particulars | Details |
|---|---|
| Company | Thermo Fisher Scientific – PPD Clinical Research |
| Job Title | Clinical Trial Coordinator – FSP |
| Job ID | R-01361221 |
| Department | Clinical Research |
| Job Type | Full-time |
| Location | Mumbai, Maharashtra, India |
| Work Arrangement | Fully remote |
| Work Schedule | Monday to Friday |
| Experience | 2+ years in global clinical trial support |
| Qualification | Bachelor’s degree preferred |
| Key Skills | Clinical trial coordination, Veeva Vault, eTMF, CTMS, clinical documentation |
| Application Mode | Online |
Job Role and Responsibilities
As a Clinical Trial Coordinator, you will support clinical study operations and work with clinical operations teams, study managers, CROs, and other project stakeholders.
Key responsibilities include:
- Providing day-to-day administrative and technical support for clinical studies.
- Reviewing essential study documents, study plans, informed consent forms, and document packets.
- Supporting regulatory inspection readiness by maintaining documentation and assisting with SOP lists and inspection preparation materials.
- Coordinating with Clinical Operations, Study Managers, study teams, and CROs to support trial activities.
- Supporting risk-based monitoring activities and related oversight.
- Participating in project meetings and preparing meeting minutes for selected studies.
- Assisting with clinical trial systems, including Clinical Trial Management System (CTMS) and Trial Master File (TMF) activities.
- Supporting site activation activities and contributing to site feasibility and site selection processes when required.
- Assisting with vendor contract administration and study close-out activities, including financial reconciliation.
- Helping onboard and train new team members when assigned.
- Completing additional project-related activities as agreed with the manager.
Eligibility Criteria and Qualifications
Candidates applying for this Clinical Trial Coordinator vacancy should review the following requirements.
Educational Qualification
A bachelor’s degree is preferred according to the employer’s recruitment announcement.
Work Experience
- At least 2 years of experience in global clinical trial support as a Clinical Trial Coordinator or Project Coordinator.
- Experience supporting Phase II and Phase III clinical studies is advantageous.
- Experience with global or international clinical trials is beneficial.
- Experience across multiple therapeutic areas, including oncology, is an advantage.
- Practical knowledge of Veeva Vault and hands-on experience with the eTMF lifecycle are important skills for this role.
Required Skills
Applicants should have strong organizational skills, attention to detail, and the ability to manage multiple tasks and changing project timelines.
Other relevant skills include:
- Knowledge of clinical trial documentation and study workflows.
- Understanding of applicable country regulations, ICH Good Clinical Practice (GCP), and relevant SOPs.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Ability to learn and work with clinical trial databases and systems.
- Good written and spoken English, along with relevant local language skills.
- Effective communication, teamwork, and independent working abilities.
- Risk identification, escalation, judgment, and decision-making skills.
- A customer-focused approach and a positive, self-motivated attitude.
Location and Work Arrangement
The position is listed under Mumbai, Maharashtra, India, with a fully remote work arrangement. The employer describes a standard Monday-to-Friday schedule. Occasional travel to site locations may be required.
Candidates should review the official vacancy details for any location, work authorization, or remote-work conditions applicable to their circumstances.
Salary and Benefits
The official recruitment details provided for this vacancy do not specify a salary range. Compensation and benefits should be confirmed through the employer’s application process.
How to Apply for Thermo Fisher Scientific Jobs
Interested and eligible candidates can apply through the official Thermo Fisher Scientific careers website.
Official application link:
https://jobs.thermofisher.com/global/en/job/R-01361221/Clinical-Trial-Coordinator-FSP
Before applying, review the complete job description and ensure that your resume highlights relevant global clinical trial experience, Veeva Vault knowledge, eTMF lifecycle experience, and clinical documentation skills.
Frequently Asked Questions
1. Is Thermo Fisher Scientific hiring Clinical Trial Coordinators in Mumbai?
Yes. The company has listed a Clinical Trial Coordinator – FSP vacancy associated with Mumbai, Maharashtra, India, under job ID R-01361221.
2. What is the required experience for this position?
The employer requires at least 2 years of experience in global clinical trial support as a Clinical Trial Coordinator or Project Coordinator.
3. What qualification is preferred for the Clinical Trial Coordinator role?
A bachelor’s degree is preferred. Relevant clinical trial coordination experience and technical knowledge are also important selection criteria.
4. Is this a remote job?
The listing identifies the position as fully remote, with Mumbai, Maharashtra, India, shown as the location. Occasional travel to site locations may be required.
5. Is Veeva Vault experience required?
The employer specifically highlights experience with Veeva Vault and hands-on experience in the eTMF lifecycle. Candidates should emphasize these skills in their applications.
6. How can candidates apply?
Candidates can review the vacancy and submit an application through the official Thermo Fisher Scientific careers link provided above.
Job Summary
| Category | Details |
|---|---|
| Company | Thermo Fisher Scientific |
| Department | Clinical Research |
| Vacancy | Clinical Trial Coordinator – FSP |
| Qualification | Bachelor’s degree preferred |
| Experience | 2+ years |
| Location | Mumbai, Maharashtra, India |
| Work Mode | Fully remote |
| Key Expertise | Global clinical trials, Veeva Vault, eTMF, CTMS |
| Application | Official company careers portal |
Disclaimer: This job information is based on the employer’s recruitment announcement. Eligibility, job status, work arrangement, and other conditions may change. Candidates should verify the latest details on the official careers website before applying.