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Responsibilities:

  • Provides regulatory guidance throughout the clinical development life cycle
  • Compiles, coordinates and reviews applications to Regulatory Authorities
  • Provides strategic regulatory input as required

Qualifications:

  • Bachelors degree in a scientific or healthcare discipline
  • 5-7 years Regulatory experience, experience leading Clinical Submissions
  • Knowledge of clinical trials methodology, protocols and indications being studied

Competencies:

  • Strong interpersonal skills and a proven ability to contribute to a team environment
  • Ability to manage multiple and varied tasks in a fast-moving environment
  • Exhibits high self-motivation and continuous improvement focuses

Precision for Medicine

Precision for Medicine integrates clinical trial execution with scientific knowledge, laboratory expertise, and data sciences, focusing on Oncology and Rare Disease. The company values employee contributions and nurtures ideas, striving for positive change.

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