Site Activation Partner III - FSP
Parexel(1 month ago)
About this role
The Site Activation Partner III at Parexel supports clinical study start-up and ethics/regulatory engagement for investigator sites within Saudi Arabia and potentially multi-country settings. The role focuses on ensuring compliant submissions to ethics committees and coordinating with internal and external stakeholders to enable timely site activation and study progress. It contributes to Parexel’s mission of advancing clinical development and improving global health.
Required Skills
- Ethics Submissions
- Site Activation
- Regulatory Submissions
- Investigator Packages
- TMF Management
- CTMS
- Document Management
- GCP Knowledge
- Stakeholder Management
- Clinical Trials
+2 more
Qualifications
- High School Diploma/GED
- Bachelor's Degree
- Master's Degree Preferred
- Fluency in Arabic
- Fluency in English
About Parexel
parexel.comFor over 35 years Parexel has been a trusted global CRO and biopharmaceutical services company. Learn more about how we can help.
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