Site Activation Partner III
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Job Description
Site Activation Partner managing clinical trial operations throughout the lifecycle of study in Saudi Arabia. Leading ethics submissions, investigator site activities, and ensuring regulatory compliance.
Responsibilities:
- Responsible for leading operational activities from start up to close out
- Drive Ethics Committee (EC) submission management activities
- Partners with local country stakeholders and/or preferred CROs
- Prepare the EC package and other associated documents
- Manage activities with Investigators sites and required documents
- Ensure timely filing of documents to electronic Trial Master File (eTMF)
- Maintain ongoing contact and communication with the study team
Requirements:
- Background in site monitoring strongly preferred
- Significant experience with study startup/initiation within industry
- Well-versed in Saudi ethics and regulatory environment
- Fluency in Arabic and English required
- Experience working in the pharmaceutical industry/or CRO in a similar role
- Experience of interacting with regulatory agency or Ethics Committee required
Benefits:
- Health insurance
- Flexible work arrangements
- Professional development opportunities
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