Clinical Trial Coordinator I/II/Senior
Posted 1 month ago
You'll complete your application on Thermo Fisher Scientific's career site.
About the Role
We are hiring a Clinical Trial Coordinator ranging from entry to senior levels to contribute to pharmaceutical services that promote global health and safety. You will play a vital role within our clinical research team by managing and supervising trial operations to guarantee that projects meet quality, budgetary, and scope expectations. Working within a worldwide organization, you will contribute to life sciences and patient health initiatives in an environment that values teamwork and individual performance. This position allows you to leverage modern technology to address complex analytical issues and enhance the efficiency of clinical development.
Requirements
- You should hold a bachelor's degree or have a minimum of four years of equivalent experience, education, and training.
- You must exhibit exceptional organizational skills, precise attention to detail, and the capability to handle various tasks amid changing project deadlines.
- You need to be proficient in English and applicable local languages, as well as the Microsoft Office suite.
- You must be self-driven, focused on the customer, and able to work both collaboratively and independently.
- You are required to gain a comprehensive understanding of local regulations, ICH Good Clinical Practices, and internal standard operating procedures.
- You must demonstrate flexibility, strong presentation skills, and the ability to successfully finalize the internal clinical training curriculum.
Responsibilities
- You will manage assigned study duties to ensure they conform to project objectives and the task matrix.
- You will manage essential study records, such as team rosters, training logs, and the electronic Trial Master File, while assisting with platforms like eTMF and GoBalto.
- You will reconcile and analyze study metrics, evaluate local regulatory paperwork, and help resolve issues related to site documentation.
- You will act as a point of contact for the project team, schedule client discussions, document meeting minutes, and aid in risk-based monitoring tasks.
- You will support the coordination of site materials, translated resources, and paperwork for Institutional Review Boards.
- You will serve as an onboarding mentor for incoming personnel and engage in departmental efforts to improve processes.
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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