Clinical trial coordinator
il y a 3 semaines
Join to apply for the Clinical Trial Coordinator - FSP role at Thermo Fisher Scientific.
Work Schedule:
Standard (Mon-Fri)
Environmental Conditions:
Office
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer.
The PPD FSP Solution: PPD's Functional Service Provider division partners with and serves as an extension of our PPD team, supporting our customers' key functions.
Clinical Trial Coordinator, client-dedicated
Our team is expanding, and we are looking to recruit a CTC to be dedicated to one client only, using and working with their systems, SOPs, and working only on the client's studies. You will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract.
Essential Responsibilities:- Clinical Trial Coordinator – Project Specialist is a key member of the Global Study Team contributing to delivering the clinical study to time, cost, and quality, and ensuring inspection readiness by taking oversight over study eTMF completeness.
- CTC role was implemented to have a broader impact on the business, by driving continuous improvement initiatives within their remit of expertise.
- Project Specialist works in close partnership with the Study Manager or Study Delivery Lead on end-to-end operational study delivery activities.
- CTC works cross-functionally, with internal and external partners, on clinical study management activities.
- CTC is responsible for monitoring study conduct and progress, identifying, resolving, and escalating risks/issues.
- CTC is responsible for reviewing key clinical documents and leading development of study plans.
- CTC is responsible for facilitating and maintaining interactions and meetings with internal and external partners.
- CTC is responsible for vendor management and CRO oversight.
- CTC is responsible for country oversight and tracking of recruitment progress.
- CTC is responsible for coordinating study-related activities and managing study team's communication.
- CTC is responsible for overseeing delivery of clinical supplies and communicating issues/risks.
- CTC is responsible for data oversight to ensure the study is inspection ready at all times.
- CTC is responsible for budget oversight – managing Task/Change Orders, expenses, tracking updates.
- CTC actively contributes to the squads as per STOM requirements.
- Graduate/Bachelor's degree in life sciences or other related field.
- Graduate or Bachelor level with at least 1+ years of relevant work experience in a pharmaceutical/scientific environment.
- Scientific background and knowledge of clinical trials and drug development process.
- Strong project management skills.
- Excellent verbal and written communication in English.
- Excellent communication and relationship-building skills.
- Opportunity to contribute to life-changing therapies.
- Comprehensive training and development programs.
- A collaborative and inclusive work environment.
- Attractive compensation and comprehensive perks.
- Work is performed in an office/laboratory/clinical and/or home office environment.
- This position is remote.
Apply today http://jobs.thermofisher.com
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