This is a hands on role, supporting Phase III studies but also could involve some Phase I work as well. This person may also have the opportunity to lead studies as they come down the pipeline in 2025 as well.

Looking for candidates with the following:

• Bachelor's degree in Life Sciences, Computer Science, or a related field.
• At least 2-3 years of experience in clinical data management or a related field.
• Familiarity with clinical trial processes and relevant regulatory guidelines.
• Proficiency in data management systems and Electronic Data Capture (EDC) tools.
• Strong attention to detail, organizational skills, and ability to work independently.
• Excellent communication and problem-solving skills.

• Experience with TMF management systems (Veeva Vault)
• Knowledge of CDISC standards and data management best practices.

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