Thermo Fisher Hiring for FSP Clinical Trial Coordinator
| Position | FSP Clinical Trial Coordinator (CTC) II |
|---|---|
| Company | Thermo Fisher Scientific |
| Location | Remote (Work From Home) |
| Experience Required | 1 Year |
| Salary | 4.5 – 6 Lacs per Annum |
| Education Requirements | B.Pharm, M.Pharm, Pharm.D, M.Sc., B.Sc., Life Sciences |
| Application Mode | Online |
| Job Highlights | Work/Life Balance, Time Management, Flexibility, Problem Solving |
| Verified Job | Yes |
FSP Clinical Trial Coordinator II at Thermo Fisher Scientific: Role Overview
The FSP Clinical Trial Coordinator (CTC) II role at Thermo Fisher Scientific offers an exciting opportunity to contribute as a Project Specialist within the clinical research domain. This remote role supports Fortrea’s PPD® clinical research portfolio and focuses on ensuring study delivery excellence by coordinating various operational aspects from the initial study setup to the final archival stage. The CTC II ensures quality control, regulatory compliance, and effective communication with stakeholders, aligning study timelines and objectives. Thermo Fisher Hiring for FSP Clinical Trial Coordinator
Key Responsibilities of CTC II
1. Study Delivery Support
- Partner with Study Managers or Delivery Leads on study setup, planning, and tracking, ensuring data accuracy within internal databases and systems.
- Oversee study progress and promptly identify any risks that could impact quality, budget, or timelines.
Thermo Fisher Hiring for FSP Clinical Trial Coordinator
2. Document and Quality Management
- Develop and review essential clinical documents such as study protocols, Informed Consent Forms (ICFs), and study plans (e.g., Monitoring, Vendor, and Risk Management Plans).
- Maintain quality and completeness within the electronic Trial Master File (eTMF), ensuring inspection readiness through regular reviews.
Thermo Fisher Hiring for FSP Clinical Trial Coordinator
3. Vendor and CRO Oversight
- Act as the primary liaison for vendor management, ensuring timely monitoring, deliverable management, and completion of outsourced activities.
4. Country and Site Oversight
- Track recruitment progress, regulatory approvals, and compliance, coordinating closely with local teams to resolve issues and maintain accurate site records.
5. Team and Communication Management
- Organize and manage study meetings, track team action items, and facilitate information flow by maintaining communication logs and distributing newsletters among stakeholders.
6. Supply and Data Oversight
- Ensure timely delivery of clinical supplies, investigational products, and study materials, addressing potential risks to maintain study continuity.
7. Budget Management
- Oversee budget elements such as task orders and expenses, aligning these with systems and agreements to ensure compliance with financial parameters.
Required Education and Experience
To qualify for the CTC II role, candidates should meet the following criteria:
- Education: Bachelor’s degree in Life Sciences or a related field.
- Experience: A minimum of 1 year of relevant experience in a clinical research or pharmaceutical environment. Familiarity with ICH-GCP guidelines and clinical study processes is essential.
Key Skills and Qualifications
- Clinical Knowledge: Foundational understanding of clinical trial processes, regulatory requirements, and industry standards.
- Project Management: Ability to manage multiple priorities, ensuring that study timelines are met effectively.
- Technical Proficiency: Knowledge of Microsoft Office (Excel, PowerPoint, Word), clinical trial management systems, and eTMF standards.
- Communication Skills: Excellent verbal and written communication skills, with an emphasis on stakeholder management and collaboration.
- Analytical and Problem-Solving Abilities: Independent thinking and a risk-based, quality-focused approach to problem-solving. Thermo Fisher Hiring for FSP Clinical Trial Coordinator
Why Consider This Role?
The CTC II role offers a unique blend of remote work flexibility and the opportunity to contribute to impactful clinical research projects. With a strong focus on work/life balance, time management, and flexibility, this role is ideal for individuals who thrive in a collaborative environment and are passionate about ensuring the success of clinical studies. Thermo Fisher Hiring for FSP Clinical Trial Coordinator
Key Benefits:
- Professional Growth: Opportunity to gain experience across various clinical trial phases.
- Remote Work: Work from home while collaborating with a global team.
- Skill Development: Enhance project management, regulatory knowledge, and vendor management skills.
Thermo Fisher Hiring for FSP Clinical Trial Coordinator
How to Apply
If you’re interested in the FSP Clinical Trial Coordinator (CTC) II position at Thermo Fisher Scientific, apply online via the company’s career portal. This role is ideal for candidates looking to advance their clinical research careers within a supportive, remote working environment.
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