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Clinical Operations Manager RWE (M/W/D)
Tasks:
Design and conduct clinical studies independently
Co-develop asset-focused Evidence Generation Plans
CRO oversight and coordination
Compliance and documentation management
Coordinate RFP process and manage vendors for study deliverables
Prioritize projects, allocate resources, and manage budgets
Collaborate with project managers and country teams for cross-country studies and timely reporting
Qualification:
Bachelor’s degree in medical, pharmacy, biological science, or equivalent experience.
Expertise in clinical and observational research methodology and technology use.
Understanding of study design and research methodologies (interventional and observational).
Knowledge of Oncology and Pharmaceutical development.
Experience with RWD and supporting multidisciplinary teams in research objectives.
Requirements:
Start: April/May 2025
Duration: 9 months
Capacity: 4-5 days per week
Location: remote
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