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Job Overview:
- Comprehensive coordination of site-level activities throughout the start-up phase.
- Ensures smooth progression from feasibility and initial outreach through to site activation.
- Proactively anticipates and mitigates issues that could delay the study
Responsibilities:
- Oversight of site level tasks associated with efficient site activation.
- Responsible for submissions to and liaise with applicable IRB/IEC.
- Perform Case Review Form (CRF) review and data validation against source documentation
Qualifications:
- University/College degree (life science preferred), or certification in a related allied health profession.
- Minimum of 3+ years of experience in clinical development or start-up/ regulatory process.
- Fluent in local official language and in English, both written and verbal
Fortrea
Fortrea helps to turn the impossible into I'm possible. They deliver exceptional service to their patients, fueled by a shared commitment to teamwork and excellence.