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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.