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Clinical Trial Coordinator
3 semanas atrás
The successful candidate will be responsible for coordinating all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations, and standard operating procedures. This role involves being a decision-maker, solving problems independently or as part of the client and ICON team.
Key responsibilities include managing competing priorities, supporting the on-site team, ensuring investigators follow the clinical trial protocol, providing training, and motivating the team to ensure high-quality results.
Key Responsibilities:
- Monitor multiple Phase I, II, III & IV clinical trial sites across different therapeutic areas.
- Assist other CRAs with co-monitoring activities both remote and on-site.
- Utilize customer service mindset with sites focusing on delivering value, building loyalty, and trust to create a positive impact and strong relationship with investigators and study coordinators.
- Collaborate with the team developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely.
- Review source data to ensure patient safety and data integrity aspect of the study.
- Act as the first point of contact for study sites escalating any concerns/issues to other departments as appropriate.
