Thermo Fisher Scientific pharma jobs for freshers hiring Clinical Trial Coordinator. Check eligibility, salary details, and apply online today now.
Introduction
If you are planning to begin your journey in clinical research, this opportunity from Thermo Fisher Scientific is a great starting point. The company is hiring freshers for the role of Clinical Trial Coordinator I under the FSP model. This remote position offers hands-on experience in global clinical trials, making it ideal for life sciences graduates who want to build a strong career in the pharma and CRO industry.
Job Overview
| Details | Information |
|---|---|
| Job Title | Clinical Trial Coordinator I (FSP) |
| Company Name | Thermo Fisher Scientific |
| Location | Mumbai, India (Remote) |
| Employment Type | Full-Time |
| Department | Clinical Research / Clinical Operations |
| Experience Required | 0–1 Year (Freshers Eligible) |
| Education | B.Pharm, M.Pharm, Pharm.D, BSc, MSc, Biotechnology |
| Salary | As per company norms |
Company Overview
Thermo Fisher Scientific is one of the world’s leading organizations in life sciences, healthcare, and clinical research services. The company collaborates with top pharmaceutical and biotechnology firms to accelerate drug discovery and development. With operations across 100+ countries and involvement in thousands of clinical trials, it provides employees with global exposure and excellent career growth opportunities.
Job Location & Employment Type
This role is based in Mumbai, India, but offers 100% remote work flexibility. Candidates can work from home while contributing to global clinical trial projects. The job is a full-time permanent position with standard weekday working hours.
Open Positions / Department Details
The vacancy is within the Clinical Trial Operations team (FSP model), where selected candidates will support sponsor-dedicated clinical projects. The role focuses on documentation management, site coordination, and trial execution support.
Key Roles & Responsibilities
As a Clinical Trial Coordinator I, your day-to-day responsibilities will include:
- Coordinating assigned clinical trial activities based on project plans
- Reviewing investigator files, regulatory documents, and eTMF records
- Supporting site activation processes and tracking timelines
- Managing clinical systems such as CTMS, Activate, and eTMF
- Processing and maintaining study-related documentation accurately
- Assisting in feasibility studies, site selection, and site tiering
- Preparing and distributing Investigator Site Files (ISF) and trial materials
- Monitoring study metrics and resolving documentation discrepancies
- Supporting audit readiness and ensuring regulatory compliance
- Coordinating with internal teams, sponsors, and clinical sites
- Maintaining vendor trackers and regulatory records
- Assisting in onboarding and training of new team members when required
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field
- Candidates with relevant diplomas and training may also be considered
Experience
- 0 to 1 year of experience in clinical research or healthcare
- Freshers are encouraged to apply
Skills Required
- Basic understanding of clinical trial processes and SOPs
- Knowledge of ICH-GCP guidelines and regulatory standards
- Strong organizational and multitasking skills
- Proficiency in MS Office tools (Word, Excel, PowerPoint)
- Good communication and documentation abilities
- Attention to detail and analytical thinking
- Ability to manage deadlines and prioritize tasks effectively
Salary & Benefits
- Salary: As per company norms
- Fully remote work opportunity
- Exposure to global clinical trials and international teams
- Learning and development programs
- Career growth in clinical research and operations
- Supportive and professional work environment
Selection Process
The hiring process typically involves:
- Online application submission
- HR screening interview
- Technical or functional interview
- Final selection and offer
How to Apply
Interested candidates can apply through the online application link provided on the official careers page of the company. Ensure your resume is updated with relevant academic and skill details.
Important Dates
- Application Deadline: Not specified (apply as soon as possible)
Why Apply for This Job?
This role is a perfect opportunity for fresh graduates aiming to enter the clinical research domain. Working with Thermo Fisher Scientific gives you access to global projects and industry best practices.
Key advantages include:
- Strong entry point into clinical research careers
- Opportunity to work remotely from anywhere in India
- Hands-on experience in real clinical trial operations
- Exposure to international regulatory frameworks
- Clear career progression into roles like CRA, Clinical Specialist, or Project Manager
FAQs
1. Who can apply for Thermo Fisher Scientific Clinical Trial Coordinator jobs?
Candidates with Life Sciences, Pharmacy, or Biotechnology degrees can apply. Freshers are also eligible.
2. Is this job work-from-home?
Yes, this is a fully remote position.
3. What is the required experience?
Candidates with 0–1 year of experience can apply, including freshers.
4. What skills are required for this role?
Basic clinical research knowledge, MS Office skills, communication, and attention to detail are essential.
5. How can I apply for this job?
You can apply online through the official application link provided by the company.
Conclusion
The Clinical Trial Coordinator I role at Thermo Fisher Scientific is a valuable opportunity for freshers to step into the clinical research field. With remote flexibility, global exposure, and strong career prospects, this role is ideal for candidates aiming to grow in the pharma industry. Apply early to secure your position.
Disclaimer
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