Trial Data Manager
Trial Data Manager – 12-Month Contract
Location: Allschwil, Switzerland
Full-time (100%) | Start: ASAP
About the Role
We are seeking an experienced Trial Data Manager to join our team in Allschwil. In this role, you will take the lead on Data Management activities for clinical studies, ensuring compliance with our clients standards, regulatory requirements, and study timelines. This is a fantastic opportunity to play a key role in advancing clinical research projects within a global healthcare leader.
Key Responsibilities
- Lead and oversee Data Management activities for assigned studies.
- Ensure data handling consistency and timely delivery of DM deliverables.
- Provide Data Management input to study protocols.
- Coordinate and oversee development of (e)CRFs, data cleaning, review tools, and database lock.
- Represent Data Management in Clinical Trial Team (CTT) meetings.
- Manage outsourced Data Management activities and partner relationships.
- Generate study metrics, reports, and ensure proper documentation and archiving.
- Contribute to SOPs, policies, and cross-functional process improvements.
- Support compliance with ICH/GCP, Quality System (QS) standards, and internal processes.
- Degree in life sciences, mathematics, statistics, informatics, or a related field.
- 3+ years’ experience in clinical research or data management within the pharmaceutical/biotech industry.
- Strong expertise in clinical trial databases, data review, data flow, and (e)CRF design.
- Knowledge of ICH/GCP and international clinical research regulations.
- Ability to lead and coordinate team activities within Data Management.
- Strong organizational, communication, and presentation skills.
- Fluent in written and spoken English.
📩 Interested?
Apply today to be part of a dynamic environment where your expertise in data management helps shape the future of clinical research.