Clinical Trials Project Coordinator
3 weeks ago
We are seeking a skilled Clinical Trials Project Coordinator to manage our existing projects. This role involves handling various responsibilities, including the preparation and submission of Clinical Trial Applications (CTAs) within the EU and globally.
Responsibilities:- Prepare and submit CTAs in EU and non-EU regions from initial preparation to notification of results.
- Review documents such as clinical study protocols, informed consent forms, and other relevant materials.
- Provide technical and practical regulatory expertise on documents and submission strategies.
- Scientific background
- 5-10 years of experience in a related field
- Proficiency in French is desirable
- Technical skills: good understanding of Clinical Trials environment, Clinical Trials regulation, CTA management through CTIS/Transition management, team coordination, word/excel/powerpoint, meeting management
The successful candidate will have the opportunity to work with a dynamic team and contribute to the success of our Clinical Trials projects. The estimated salary for this position is $80,000 - $110,000 per annum, depending on qualifications and experience.
This role offers a chance to grow professionally and develop expertise in Clinical Trials project management. If you are a motivated and organized individual with a passion for Clinical Trials, we encourage you to apply.
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