Our ideal candidate will have the following:
Qualifications:
- Bachelor’s degree in life sciences, health sciences, or related field. A Master's degree or certification in Clinical Data Management (CDM) is a plus.
- Proven experience (8+ years) in clinical data management within the pharmaceutical, biotechnology, or CRO industries. Lead experience with Global Phase III studies is required.
- Proficiency with Veeva (Vault eTMF) and other clinical data management software (e.g., EDC systems, SAS).
- Solid understanding of clinical trial processes, ICH/GCP guidelines, and FDA/EMA regulations.
- Strong analytical, organizational, and problem-solving skills.
- Excellent communication skills and ability to work in a team-oriented environment.
...