Medical Monitor
2 weeks ago
Job_Responsiblities
- Advise clients, project teams, sites, data safety monitoring boards, regulatory agencies and thirdparty vendors on medical matters
- Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations
- Review and analysis of clinical data to ensure the safety of study participants in clinical studies
- Ensure that the reported data is accurate, complete, and verifiable and that the conduct of the trial is in compliance with the currently approved protocol/amendments.
- Medical Background
- Min. Two years of experience with Oncology background is a must
- Full working proficiency in English
- Communication, presentation and analytical skills
- Problemsolving, team and detailoriented
Ability to commute/relocate:
- Riyadh: Reliably commute or planning to relocate before starting work (required)
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