[Work From Home] FSP Clinical Trial Coordinator at Thermo Fisher Scientific

[Work From Home] FSP Clinical Trial Coordinator at Thermo Fisher Scientific

Position	FSP Clinical Trial Coordinator (Work From Home)
Organization	Thermo Fisher Scientific
Qualification	B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences
Experience	1-3 years
Location	Work From Home
Salary	Not Disclosed
Key Skills	eTMF expertise, ICH GCP, MS Office, Regulatory Submissions
Role Type	Administrative and Technical Support
Key Responsibilities	Managing trial documents, supporting site activation, tracking activities, regulatory submissions

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Exciting Opportunity: FSP Clinical Trial Coordinator at Thermo Fisher Scientific

Are you passionate about contributing to groundbreaking clinical research while enjoying the flexibility of working from home? Thermo Fisher Scientific, a global leader in the life sciences and healthcare sector, is offering a remote opportunity for an FSP Clinical Trial Coordinator. This role is perfect for individuals who are looking to make a significant impact in the world of clinical trials while balancing the convenience of remote work. [Work From Home] FSP Clinical Trial Coordinator at Thermo Fisher Scientific

Join a Global Leader in Clinical Research

Thermo Fisher Scientific’s Functional Service Provider (FSP) team is at the forefront of clinical research services, driving innovation and bringing new treatments to life. As part of the prestigious PPD® clinical research portfolio, the FSP team partners with leading organizations worldwide to develop solutions for some of the most pressing healthcare challenges.

As an FSP Clinical Trial Coordinator, you’ll work on pivotal clinical trials, supporting the project team to ensure the successful activation and management of trial sites. If you’re someone who thrives in a dynamic and collaborative environment, this role could be your next career step.

Your Key Responsibilities

In this role, you’ll be responsible for multiple tasks that are crucial to the success of clinical trials. Your day-to-day duties will include:

• Administrative and technical support: You will assist the project team in coordinating trial activities, providing essential support for the smooth execution of clinical research.
• File and document review: To ensure compliance with clinical trial regulations and readiness for audits, you’ll review internal, country-specific, and investigator files regularly.
• Managing essential trial documents: You will organize and process critical documents within the electronic Trial Master File (eTMF), a vital system for clinical trials.
• Coordinating non-clinical study materials: Part of your job will involve ensuring that important materials such as Investigator Site Files (ISF) and Pharmacy binders are delivered accurately and on time.
• Supporting regulatory submissions: You will play an important role in assisting regulatory submissions, maintaining study-specific documentation, and tracking project activities.
• Collaborating with internal teams: You’ll work closely with various departments to align site start-up activities with project timelines, addressing any potential risks or issues that arise during the process.

This multi-faceted role is both challenging and rewarding, offering plenty of opportunities to sharpen your project management skills while contributing to the development of new medical treatments.

What Qualifications Do You Need?

Thermo Fisher is looking for candidates with the following qualifications to ensure success in this role:

• Educational background: A Bachelor’s Degree in Life Sciences is preferred, but related degrees in pharmacy or medical fields (B.Pharm, M.Pharm, Pharm.D, etc.) are also accepted.
• Experience: You should have 1-3 years of relevant experience as a Clinical Research Coordinator (CRC) or Clinical Trial Coordinator (CTC).
• Knowledge of regulations: Familiarity with ICH Good Clinical Practices (GCP) and clinical research regulations is crucial for this role.
• Communication skills: Excellent English communication skills (both oral and written) are essential, as you will be dealing with multiple stakeholders.
• eTMF expertise: Having a solid understanding of electronic Trial Master File (eTMF) systems is a must.

Key Skills for Success

The ideal candidate will have a blend of organizational and interpersonal skills, as well as technical proficiency. Here’s what you’ll need to excel:

• Attention to detail: Given the high stakes of clinical trials, you’ll need to be detail-oriented to manage multiple tasks and documents effectively.
• Tech-savviness: You’ll work with software like MS Office and clinical trial databases, so proficiency with Word, Excel, and PowerPoint is important.
• Customer service orientation: Trials are high-pressure environments, and you’ll need to work well with other departments and manage risks effectively.
• Team collaboration: While you’ll be working remotely, you’ll need to collaborate closely with internal teams, making good communication skills essential.
• Regulatory navigation: You should be able to handle regulatory requirements and support site capacity management for a smooth trial process.

This position is not just a job; it’s an opportunity to advance medical research and positively impact patient care globally. If you have a passion for clinical trials and are ready to bring your expertise to a company like Thermo Fisher, this could be the perfect role for you!

Ready to make a difference? Apply today!