VACANCY
Clinical Data Manager: Senior
What we’re looking for
- Strong experience in Clinical Data Management within a CRO, pharmaceutical or biotech environment
- Experience managing clinical studies independently
- Good knowledge of GCP, clinical data standards and regulatory requirements
- Experience with EDC systems and clinical database processes
- Strong organizational and problem-solving skills
- Ability to communicate effectively with clients and cross-functional teams
- Professional working proficiency in English
We are particularly interested in people who combine strong technical CDM expertise with ownership, client communication and practical problem-solving.
At Valos, you will work in a specialized biometrics environment where experienced professionals have direct impact on projects, clients and how we develop our services.
The role
As a Senior Clinical Data Manager, you will take ownership of clinical data management activities across international clinical studies and work directly with sponsors, internal biometrics teams, and external partners.
Key responsibilities include:
- Leading end-to-end Clinical Data Management activities
- Developing and reviewing DMPs, CRFs/eCRFs, edit checks and data review specifications
- Managing database build, UAT, data cleaning and database lock activities
- Coordinating data reconciliation and external data transfers
- Monitoring data quality, timelines and study deliverables
- Working closely with Biostatistics and Statistical Programming teams
- Communicating directly with sponsors and supporting study-level decisions
- Contributing to the continuous improvement of CDM processes and standards
