Job Description

• Be the primary site contact and site manager throughout the study lifecycle, taking overall accountability for assigned sites
• Build, nurture, and maintain strong site relationships to ensure stable performance from start-up through close-out
• Perform remote and on-site monitoring in accordance with ICH-GCP, local regulations, protocol, monitoring plans, and our organization’s SOPs
• Ensure high-quality data: complete, accurate, unbiased—and always with participant rights, safety, and well-being protected
• Conduct all site visit types (validation, initiation, monitoring, close-out), with timely, clear, and comprehensive reporting
• Drive site readiness: coordinate cross-functional activities and contribute to site selection and validation
• Oversee regulatory documentation across start-up, maintenance, and close-out; ensure accuracy and timeliness
• Identify, assess, and resolve site performance, quality, and compliance issues; escalate per the CRA Escalation Pathway when needed in collaboration with the CRA Manager, CRM, TA Head, and CRD
• Partner across functions (country operations, finance, regulatory affairs, pharmacovigilance, legal, regional operations, HQ) and with external stakeholders (vendors, IRBs/IECs, Regulatory Authorities)
• Maintain accurate, on-time documentation in CTMS, eTMF, and related systems
• Share expertise as a process SME; mentor/buddy peers and contribute to team best practices
• Support or lead audit/inspection activities; conduct co-monitoring as appropriate
• Expand our research network: identify and develop new potential sites per country strategy, strengthening local research capabilities

• Demonstrated experience in clinical monitoring/site management within biopharma, CRO, or academic research
• Strong working knowledge of ICH-GCP, local regulations, and clinical trial operations
• Proven ability to manage multiple sites, priorities, and stakeholders with a solutions-focused mindset
• Exceptional communication and relationship-building skills with investigators and site staff
• High attention to detail, documentation excellence, and proficiency with CTMS, eTMF, and digital monitoring tools
• Proactive problem-solving with sound judgment and timely escalation when needed
• Bachelor’s degree in life sciences or related field (advanced degree a plus)

• Meaningful impact: contribute directly to advancing clinical science and patient outcomes
• Growth and mentorship: act as a subject matter expert, mentor peers, and shape best practices
• Collaborative culture: work cross-functionally with supportive, high-performing teams
• Future-facing operations: leverage modern systems and monitoring approaches to deliver operational excellence

Closing date for applications :23/01/2026

Required Skills:

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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