
Clinical Trial Coordinator
Posted 8 hours ago
You'll complete your application on Thermo Fisher Scientific's career site.
About the Role
This Clinical Trial Coordinator position functions as a key administrative and technical resource, assisting project teams throughout the entire duration of clinical studies. As a central point of contact for interdisciplinary groups, you will supervise routine project operations, facilitate site launches, and handle core study records. You will contribute significantly to the successful delivery of trials according to schedule and financial parameters, ensuring strict adherence to quality and regulatory guidelines. By working in this international scientific setting, you will aid in creating innovative medical treatments and health products. You will navigate intricate, matrix-style organizations where both collaborative efforts and personal drive are essential, handling tasks from client communication to data analysis to ensure the operational success of biotech and pharmaceutical initiatives.
Requirements
- You should hold a minimum of a high school diploma or its equivalent, while a bachelor's degree is preferred.
- At least six years of related work experience providing the expertise needed for clinical trial management is required, or a suitable mix of schooling and direct practice.
- You must be proficient in MS Office, possess strong English proficiency, and be capable of learning proprietary clinical trial database software.
- You need to show strong organizational abilities, extreme attention to detail, and the capacity to interpret complicated project information.
- A thorough knowledge of ICH Good Clinical Practices, regional regulations, and medical terminology is necessary, alongside the ability to mitigate risks and function within a matrix-style work structure.
- Strong communication and interpersonal talents are needed to collaborate and negotiate with clients, investigators, and colleagues.
Responsibilities
- You will oversee trial-related operations, keep study records precise, and ensure all work adheres to designated matrices and quality benchmarks.
- Your duties include managing specific software, tracking tools, and databases, along with performing internal and investigator file audits to guarantee constant preparedness for inspections.
- Supporting site activation involves creating critical timelines, assisting with regulatory filings, and updating site information.
- You will assist with worldwide feasibility assessments, evaluate site capabilities, and interview physicians by phone concerning protocols.
- Responsibilities include mentoring incoming personnel, acting as a resource for issue escalation, and handling vital trial paperwork including eTMF reviews and translated content.
- You will coordinate meetings with clients, document discussions, and track performance indicators to verify that project timelines and budgets are met.
Benefits & Perks
- The role is fully remote with a standard schedule of Monday to Friday.
- You will be provided with comprehensive onboarding support and a clinical training curriculum to aid your career growth.
- Although the position is remote, you may be required to travel occasionally.
Note: This listing is summarized and paraphrased by WorkNow from a publicly posted role. For the original wording and full details, please refer to the employer's official posting.
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