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Are you looking for clinical research jobs in India? 🔬 Thermo Fisher Scientific has a Clinical Trial Coordinator – FSP job listing under reference number R-01361221, associated with Mumbai, Maharashtra, India. The opportunity is listed as a full-time position with a fully remote work arrangement.
This opportunity may interest professionals seeking careers in clinical trial coordination, clinical operations, and regulated healthcare research. Candidates with strong organizational skills, attention to detail, computer proficiency, and an understanding of clinical research procedures may wish to explore the vacancy.
Clinical trial coordinators help support clinical research activities by managing assigned tasks, maintaining accurate documentation, coordinating project activities, and following established procedures. These responsibilities contribute to the effective execution of clinical studies.
If you are interested in Clinical Trial Coordinator jobs in Mumbai in 2026, read the job details, skills, work arrangement, and application instructions below before applying.
📌 Clinical Trial Coordinator Job Details 2026
Here is a summary of the available recruitment information.
| Job Detail | Information |
|---|---|
| Job Title | Clinical Trial Coordinator – FSP |
| Company | Thermo Fisher Scientific |
| Job Reference Number | R-01361221 |
| Job Location | Mumbai, Maharashtra, India |
| Job Type | Full-time |
| Work Arrangement | Advertised as fully remote |
| Job Category | Clinical Research |
| Industry | Healthcare and Clinical Research |
| Salary | Not confirmed in the available information |
| Educational Qualification | Verify in the official job description |
| Experience Required | Verify in the official job description |
| Application Deadline | Not confirmed |
| Official Application Link | Available below |
Important: The information above summarizes the vacancy details supplied for this article. Candidates should consult the official recruitment page to confirm the current vacancy status, qualifications, experience requirements, salary, and other employment conditions.
🔬 About the Clinical Trial Coordinator Role
A Clinical Trial Coordinator supports activities associated with the planning, organization, documentation, and execution of clinical research projects.
Clinical trials are conducted to evaluate the safety and effectiveness of investigational medicines, medical devices, and other healthcare interventions. These studies require coordination among clinical research teams, investigators, sponsors, clinical sites, and other stakeholders.
Depending on the project and employer, clinical trial coordination responsibilities may include:
- Supporting clinical trial documentation and administrative activities.
- Maintaining accurate study records and project trackers.
- Coordinating assigned tasks with internal teams.
- Reviewing information for completeness and accuracy.
- Following applicable standard operating procedures.
- Supporting compliance with Good Clinical Practice requirements.
- Monitoring assigned activities and project timelines.
- Identifying potential issues and escalating them appropriately.
- Communicating with relevant stakeholders.
- Using electronic systems to manage clinical research information.
These are examples of responsibilities commonly associated with clinical trial coordination. Applicants should review the official job description to identify the specific duties associated with this vacancy.
📝 Skills Required for Clinical Trial Coordinator Jobs
Candidates interested in clinical research coordination should assess their skills against the requirements specified in the official recruitment listing.
The available job information highlights several important professional competencies.
1. Organizational and Time Management Skills
Clinical research projects involve multiple activities, documents, deadlines, and stakeholders. Strong organizational skills help professionals manage their responsibilities efficiently.
Candidates should be comfortable prioritizing tasks, maintaining accurate records, tracking pending activities, and completing assigned work within established timelines.
Effective time management is particularly important when several project activities must be coordinated simultaneously.
2. Knowledge of Clinical Research Regulations
Understanding clinical research regulations and quality requirements is important when working in a regulated research environment.
Relevant areas of knowledge may include:
- ICH-GCP: International ethical and scientific quality standards for clinical trials.
- Standard Operating Procedures (SOPs): Documented procedures that guide consistent work practices.
- Country-specific regulations: Applicable legal and regulatory requirements governing clinical research.
- Work Practice Documents (WPDs): Work instructions and procedural guidance used by an organization or project.
- Clinical trial documentation: Procedures for maintaining complete, accurate, and traceable study records.
Candidates should be willing to learn and follow applicable regulations, company procedures, and client-specific requirements.
3. Computer and Microsoft Office Skills
Computer proficiency is valuable for professionals working in clinical research operations.
Candidates may benefit from familiarity with the following applications:
Microsoft Word: Preparing, reviewing, and formatting documents.
Microsoft Excel: Maintaining trackers, organizing information, and reviewing data.
Microsoft PowerPoint: Preparing presentations and communicating project information.
The ability to learn clinical trial databases and electronic documentation platforms is also valuable.
The exact software systems required for this position should be confirmed through the official job description.
4. Data Review and Attention to Detail
Clinical research requires accurate documentation and careful handling of study information.
Professionals working in coordination roles may need to review records, identify inconsistencies, maintain trackers, and follow established processes for resolving issues.
Strong attention to detail helps support documentation quality and reduces the risk of avoidable errors.
5. Communication and English Language Skills
Clear communication is important when coordinating clinical research activities.
Depending on the position, professionals may communicate with colleagues, clients, clinical research teams, and other stakeholders.
Candidates should be able to understand instructions, communicate project updates, prepare professional documentation, and escalate issues clearly.
The recruitment information also refers to local-language proficiency where necessary. Applicants should verify the specific language requirements for this position.
6. Teamwork and Independent Working
Clinical research professionals often collaborate with colleagues across different departments and project teams.
At the same time, they may be expected to complete assigned activities independently and manage their workload without continuous supervision.
The ability to work collaboratively while taking responsibility for individual tasks can be valuable in a remote working environment.
7. Problem-Solving and Risk Management
Clinical trial projects may encounter unexpected issues, competing priorities, and changing timelines.
Candidates should be able to recognize potential problems, assess available information, follow established procedures, and escalate issues when appropriate.
Good judgment and a structured approach to problem-solving help support project coordination and operational efficiency.
8. Flexibility and Adaptability
Clinical research requirements can change according to project needs, stakeholder requests, and operational priorities.
Professionals should be comfortable adjusting their schedules, reprioritizing tasks, and learning new systems or procedures when required.
Maintaining accuracy and quality while adapting to changing circumstances is an important professional skill.
9. Interpersonal and Coordination Skills
Clinical trial coordination involves working with different individuals and teams.
Positive interpersonal skills can help professionals clarify expectations, coordinate activities, communicate deadlines, and maintain productive working relationships.
Candidates should also be comfortable asking questions, providing updates, and raising concerns through appropriate channels.
10. Willingness to Complete Clinical Training
Clinical research organizations may provide training covering company procedures, project-specific requirements, quality standards, and regulatory expectations.
Candidates should be willing to complete the required training and demonstrate that they can apply the relevant procedures to their assigned responsibilities.
The precise training requirements for this vacancy should be verified with the employer.
🏠 Is This a Work-From-Home Clinical Research Job?
The vacancy information supplied for this article describes the Clinical Trial Coordinator – FSP position as fully remote.
This makes the opportunity worth exploring for candidates interested in remote clinical research jobs in India.
Remote clinical research professionals may use approved electronic systems, participate in virtual meetings, maintain digital documentation, and coordinate activities with colleagues online.
However, applicants should read the official listing carefully because the job information also mentions possible occasional visits to clinical site locations and potential travel.
Before applying, confirm the following points:
- Whether the position can be performed entirely from home.
- Whether candidates must reside in Mumbai or another specified location.
- Whether occasional visits to clinical sites are required.
- How frequently business travel may occur.
- Whether any specific working hours or shift arrangements apply.
- Whether the employer provides the necessary equipment and remote-working support.
Important: A remote designation does not necessarily mean that there are no location restrictions or travel requirements.
🎯 Who Can Apply for This Clinical Trial Coordinator Vacancy?
This opportunity may be relevant to professionals interested in clinical research operations and clinical trial coordination.
However, the exact educational qualifications and minimum experience required have not been independently established from the information available for this article.
Before applying, candidates should verify whether the employer requires:
- A degree in pharmacy, life sciences, nursing, or another relevant discipline.
- Previous clinical research or clinical operations experience.
- Knowledge of ICH-GCP and clinical trial regulations.
- Experience using clinical trial databases or electronic systems.
- Proficiency in Microsoft Office applications.
- Strong written and verbal communication skills.
- The ability to work independently in a remote environment.
These are areas to check, not confirmed mandatory eligibility criteria for this particular vacancy.
Applicants should rely on the official recruitment listing when determining whether they meet the requirements.
📚 How to Prepare for a Clinical Trial Coordinator Job
Candidates interested in clinical research careers can strengthen their professional profiles by developing relevant knowledge and practical skills.
Learn Good Clinical Practice
Understand the purpose of ICH-GCP, participant safety, informed consent, investigator responsibilities, documentation, and clinical trial quality.
Understand Clinical Trial Documentation
Become familiar with the purpose of essential clinical trial documents, study records, and documentation quality checks.
Improve Microsoft Excel Skills
Learn how to organize data, use filters, apply basic formulas, maintain trackers, and identify inconsistencies in spreadsheets.
Develop Professional Communication Skills
Practice writing clear emails, preparing concise status updates, documenting tasks, and communicating potential delays.
Learn Clinical Research Terminology
Understand commonly used terms such as clinical trial protocol, investigator, sponsor, clinical research organization, informed consent, adverse event, and study closeout.
Prepare Your Resume
Highlight relevant experience, education, computer skills, clinical research training, documentation responsibilities, and coordination activities.
Candidates should describe their qualifications accurately and avoid claiming experience or competencies they do not possess.
🚀 Career Opportunities in Clinical Research
Clinical research offers a range of potential career paths for individuals interested in healthcare research and clinical operations.
Depending on their education, experience, and professional development, candidates may explore roles such as:
- Clinical Trial Coordinator
- Clinical Trial Assistant
- Clinical Research Coordinator
- Clinical Operations Associate
- Clinical Trial Management Associate
- Clinical Study Start-Up Associate
- Clinical Research Project Coordinator
- Clinical Research Project Manager
These roles have different responsibilities and eligibility requirements. Progression depends on individual qualifications, practical experience, employer requirements, and available opportunities.
Developing expertise in clinical trial documentation, regulatory compliance, project coordination, and clinical research systems can help professionals prepare for relevant positions.
📩 How to Apply for Clinical Trial Coordinator Jobs in Mumbai
Interested candidates can review the official Thermo Fisher Scientific recruitment listing using the job reference number R-01361221.
Official Application Link
Company: Thermo Fisher Scientific
Position: Clinical Trial Coordinator – FSP
Job Reference: R-01361221
Location: Mumbai, Maharashtra, India
Work Arrangement: Advertised as fully remote
Apply Online: https://jobs.thermofisher.com/global/en/job/R-01361221/Clinical-Trial-Coordinator-FSP
Steps to Apply
- Open the official recruitment link provided above.
- Check whether the vacancy is still accepting applications.
- Read the complete job description carefully.
- Verify the educational qualifications and experience requirements.
- Confirm the remote-working arrangements and any travel requirements.
- Update your resume to highlight relevant skills and experience.
- Complete the application through the employer’s official recruitment portal, following the instructions provided.
- Keep a record of your application for future reference.
Application deadline: Not confirmed in the information available for this article. Check the official recruitment portal for the latest details.
Candidates should apply only through the official employer’s recruitment channel and should verify any requests for personal or financial information before responding.
❓ Frequently Asked Questions (FAQs)
1. Is there a Clinical Trial Coordinator job vacancy in Mumbai in 2026?
A Clinical Trial Coordinator – FSP listing with reference number R-01361221 has been identified on the Thermo Fisher Scientific recruitment website. Check the official listing to confirm whether applications are currently open.
2. Is this a work-from-home clinical research job?
The opportunity is described as fully remote in the available recruitment information. However, applicants should confirm any location restrictions, clinical site visits, or travel requirements in the official job description.
3. What is the salary for this Clinical Trial Coordinator position?
The salary has not been confirmed in the information available for this article. Candidates should check the official listing or contact the employer’s recruitment team for compensation details.
4. What qualifications are required for this job?
The exact educational qualifications have not been confirmed here. Review the official job description to determine the required degree, relevant experience, and other eligibility criteria.
5. Is prior clinical research experience necessary?
The minimum experience requirement has not been established from the information available for this article. Applicants should check the official listing before deciding whether to apply.
6. What is the job reference number?
The job reference number is R-01361221.
7. How can I apply for this vacancy?
Visit the official Thermo Fisher Scientific recruitment page:
https://jobs.thermofisher.com/global/en/job/R-01361221/Clinical-Trial-Coordinator-FSP
👉 Explore the course on Udemy:
https://trk.udemy.com/c/6907719/3193860/39854
Review the complete job description and follow the application instructions provided by the employer.
8. What skills are useful for a Clinical Trial Coordinator?
Useful skills include organization, attention to detail, professional communication, Microsoft Office proficiency, clinical research knowledge, documentation accuracy, time management, and problem-solving.
The specific skills required for this vacancy should be confirmed through the official job description.
⭐ Final Thoughts
The Clinical Trial Coordinator – FSP opportunity in Mumbai may interest professionals seeking careers in clinical research and clinical operations.
The available recruitment information describes the position as full-time and fully remote, while highlighting competencies such as organization, communication, computer proficiency, regulatory awareness, and problem-solving.
Before applying, carefully review the official job description to confirm the vacancy status, eligibility requirements, experience criteria, salary information, and remote-working conditions.
If your qualifications and experience match the employer’s requirements, consider submitting your application through the official recruitment portal.
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