Clinical Trial Accelerator
1 week ago
We are seeking an experienced and agile Clinical Research Associate who is driven by accelerating the start-up of globally run clinical trials. The successful candidate will be motivated in making a difference in reimagining medicine.
Key Responsibilities- Accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I-IV GDD trials within the country.
- Proactive site preparation and early identification of real site needs and issues.
- Close handover to execution CRA for all sites, from issue management to risk identification.
The Study Start-Up CRA will work directly with the local clinical research team and reports to the SSU Team Lead. They will support country SSU strategy in close collaboration with SSO Study Start-Up Team Lead, SSO Study Start-Up Manager, SSO Feasibility Manager as well as SSO Site Partnership Manager.
Requirements- A degree in scientific or health discipline, preferably with clinical operations experience.
- Minimum 3 years' experience in clinical operations in a monitoring / site management role.
- Advanced understanding of all aspects of clinical drug development with particular emphasis on trial set-up, execution, and monitoring.
- Strong site management capabilities with demonstrated negotiating and problem-solving skills.
- Bilingual: English and French.
- Central/in-house monitoring or field monitoring experience.
The salary range for this position is estimated at $85,000 - $110,000 per year, depending on qualifications and experience. This role is eligible for remote work arrangements and we offer a competitive benefits package.
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