Senior Site Manager
On-siteJohannesburg, Gauteng, South Africa
Job Summary
Act as the primary local contact for assigned sites, executing site initiation, monitoring (including remote), and close-out per SOPs. Manage site activation with the central team, oversee recruitment strategy, and ensure adequate supply storage and inventory. Train site staff, resolve data queries, and guarantee accurate data entry and reporting of Adverse Events. Maintain complete documentation, conduct file reviews, and collaborate on CAPAs for quality issues. Track site costs, prepare for close-out visits, and mentor less experienced managers. Travel up to 75% of the time. Requires a Life Sciences degree, 3+ years clinical trial monitoring experience, and proficiency in English and the local language.
Required Qualifications
- Matric (Grade 12)
- A minimum of a BA or BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience)
- A minimum of 3 years of clinical trial monitoring experience
- Strong understanding of GCP, company SOPs, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines
- Strong IT Skills In Appropriate Software And Company Systems
- Willingness to travel up to 75% with occasional overnight stay away from home
- Proficient in speaking and writing the country language and English
- Good written and oral communication
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