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.

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Contract work,