BelgradeFull TimeOperations
Remotely
gcpclinical researchregulatory affairsvaultichixrs
Job Description
📋 Description
- Drive start-up and maintenance activities for assigned studies/sites.
- Develop country/site activation plans with risk mitigation.
- Coordinate with regulatory/CTS for CA submissions and approvals.
- Manage site activation with contract manager, Site Monitor, and Leads.
- Trigger IP shipments, issue green light letters, and activate sites in IXRS.
- Maintain SSU KPIs and audit readiness; ensure policy compliance.
🎯 Requirements
- Bachelor's degree in health care or science preferred, or equivalent experience.
- 1-2 years in clinical research; 1+ year in study start-up management (region).
- Experience with remote/virtual teams and strong interpersonal skills.
- Working knowledge of ICH/GCP and local regulatory environment.
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