Clinical Trial Manager
Há 3 dias
Medpace, Inc. is seeking a full-time Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo. This role plays a key part in the clinical trial management process, utilizing expertise to develop and grow a career in a dynamic environment.
Key Responsibilities:- Efficiently manage and successfully execute clinical trial submissions.
- Collaborate with cross-functional teams to ensure timely and accurate submissions.
- Develop and maintain regulatory knowledge to stay up-to-date with industry requirements.
- Proven experience in clinical trial management or regulatory affairs.
- Strong understanding of regulatory submissions and clinical trial operations.
- Excellent communication and project management skills.
At Medpace, we offer a dynamic work environment, opportunities for growth and development, and a commitment to excellence in clinical research.
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