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Main Responsibilities:
- Provide medical expertise and lead the design and implementation of clinical development strategies.
- Lead the development of clinical trial protocols, ensuring scientific rigor and compliance with global regulatory requirements.
- Provide study leadership and collaborate with cross-functional team members across the study lifecycle.
Knowledge, Abilities & Experience:
- Advanced scientific degree (MD, PhD, or PharmD) required.
- Must have 5+ years of clinical research and/or drug development experience.
- Experienced in designing and conducting Phase I-III clinical trials and regulatory submissions.
Key Technical Competencies:
- Objective-driven, solution and results oriented, with a sense of urgency.
- Ability to thrive in a fast-paced and dynamic environment.
- Excellent verbal, written, and interpersonal communication skills.
Ipsen Biopharmaceuticals Inc.
Ipsen is a mid-sized global biopharmaceutical company focused on transformative medicines in Oncology, Rare Disease, and Neuroscience. With nearly 100 years of experience and global hubs in the U.S., France, and the U.K, they are committed to a culture of collaboration, excellence, and impact and empower every individual to be their true selves and grow alongside the company’s success.