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 (5+ years) in clinical data management within the pharmaceutical, biotechnology, or CRO industries. Phase III expeirence is helpful
- 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.
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