Senior Project Data Manager role in Basel, CH, for CTC Resourcing Solutions AG. Requires 5+ years in clinical data management, a master’s in life sciences or related field, and Swiss/EU citizenship or work permit. On-site contract position with focus on clinical trial data management, vendor oversight, and team leadership.
This role is responsible for overseeing data management activities throughout clinical trials, ensuring data integrity, regulatory compliance, and efficient project execution from study initiation to database lock and archiving.
Responsibilities
- Lead data management efforts across clinical trials, from setup to final archiving.
- Manage project timelines, ensuring milestones are met from study initiation to database lock.
- Contribute to protocol development, CRF design, SAP, and Clinical Study Reports.
- Oversee data review, cleaning, and quality control processes.
- Coordinate testing and deployment of electronic data capture systems (eCRF).
- Manage external vendors, including selection, performance monitoring, and budget oversight.
- Set performance goals and supervise direct reports.
- Maintain accurate documentation, ensure audit readiness, and oversee data archiving.
Requirements
- Must hold a Swiss working/residency permit or be a Swiss/EU citizen.
- Master’s degree in life sciences, statistics, mathematics, informatics, or a related field.
- Minimum of 5 years of experience in clinical data management within pharma or biotech.
- Strong understanding of clinical trial workflows, data flow, and eCRF design.
- In-depth knowledge of ICH-GCP and regulatory standards.
- Experience with clinical databases and data review tools.
- Proven leadership and project management abilities.
- Excellent communication and stakeholder management skills.
- Fluent in English, both written and spoken.
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