Clinical Trial Coordinator II Position at Thermo Fisher Scientific in Mumbai | Remote
A rare chance for experienced clinical trial professionals to join Thermo Fisher Scientific as a Clinical Trial Coordinator II. This fully remote role is based in Mumbai and seeks candidates with over two years of relevant experience in clinical trial coordination and related activities.
About The Company
Thermo Fisher Scientific is a global leader in serving science, providing a wide range of innovative solutions for laboratories and research institutions. The company operates in the life sciences sector, focusing on advancing scientific discovery and improving patient outcomes through its comprehensive portfolio of products and services. With a commitment to quality and innovation, Thermo Fisher supports clinical research and development on a global scale.
- Company: Thermo Fisher Scientific
- Position: Clinical Trial Coordinator II / Clinical Operations Delivery Associate II
- Job Type: Full Time
- Work Mode: Fully Remote
- Location: Mumbai, India
- Schedule: Monday–Friday
- Experience: 2+ years comparable CTC experience
- Qualification: Bachelor’s degree preferred
- Key Systems: Veeva eTMF, CTMS
- Job Requisition ID: R-01367751
Job Description
The Clinical Trial Coordinator II will provide administrative and technical support to clinical project teams and contribute to trial activities throughout site activation and study execution. Responsibilities include maintaining trial documentation, supporting site activation, tracking regulatory documents, and assisting with feasibility activities. The role requires strong organizational skills to manage multiple study activities and documentation requirements simultaneously.
Clinical Trial Coordinator II Responsibilities
- Coordinate, oversee and complete assigned clinical trial activities according to the applicable task matrix.
- Perform department, internal, country and investigator file reviews.
- Document findings in the appropriate clinical trial systems.
- Ensure assigned activities are completed on time and to required quality standards.
- Process documents for client electronic Trial Master File (eTMF) systems.
- Review and track local regulatory documentation.
- Assist with resolving site documentation findings.
- Maintain vendor trackers.
Eligibility Criteria
- Bachelor’s degree preferred.
- Previous Clinical Trial Coordinator (CTC) experience.
- Experience comparable to at least 2 years as a CTC.
- Hands-on experience with Veeva eTMF and CTMS.
- Experience working on global clinical trials.
Required Skills
- Clinical trial coordination and operations knowledge.
- Documentation skills and stakeholder-management abilities.
- Communication and presentation skills.
- Attention to detail and problem-solving skills.
- Ability to work independently and in a matrix environment.
Salary
Thermo Fisher Scientific has not disclosed the compensation range in the supplied job posting. Candidates should confirm compensation directly with the employer during the recruitment process.
How to Apply
Interested candidates can apply through the official Thermo Fisher Careers portal: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE.
This Clinical Trial Coordinator II opportunity at Thermo Fisher Scientific is ideal for professionals seeking to advance their careers in clinical trial coordination. Interested candidates are encouraged to apply before the deadline to seize this opportunity in a leading global company.
