Director of Clinical Development - Permanent - Princeton

Proclinical is seeking a Medical Director of Clinical Development Gastroenterology to join a globally recognized pharmaceutical company.

Primary Responsibilities:

The successful candidate will report to the Vice President & Head of Clinical Development and play a crucial role in shaping the clinical development strategy for branded medicines.

Skills & Requirements:

• MD, or MD/PhD qualification.
• Experience in biotech and/or pharma drug development.
• Proven ability to develop unique and innovative clinical strategies.
• Experience in designing and developing platform trials, randomized phase 2 and registrational Phase 3 programs.
• Prior experience interacting effectively with regulatory agencies.
• Solid knowledge of compliance and global regulatory requirements (ICH) for development of pharmaceutical candidates/products.
• Effective written and verbal communications and interpersonal skills.
• Strong consensus-building skills and the ability to lead multi-disciplinary teams.
• Experience in working with external collaborators, including CROs, national institutes and multinational pharmaceutical companies.
• Strong analytical and problem-solving skills, well organized and detail oriented.

The Medical Director - Clinical Development Gastroenterology responsibilities will be:

• Contribute to the clinical development strategy, aligning with the company's overall goals and objectives.
• Design, oversee, and manage clinical trials to evaluate the safety and efficacy of investigational products.
• Provide scientific leadership for the clinical portfolio.
• Provide recommendations and insights on study feasibilities within the therapeutic area.
• Serve as a key external spokesperson for clinical programs.
• Support implementation of initiatives and program-level activities specific to the therapeutic area of focus.
• Collaborate across multiple internal multidisciplinary functions.
• Support interactions with regulatory authorities and data monitoring boards.
• Support the design and implementation of clinical protocols, data collection systems, and data analysis.
• Implement best practices and standards for trial management.
• Foster collaboration with cross-functional teams.
• Establish and maintain relationships with key opinion leaders, clinical investigators, and other external partners.

If you are having difficulty in applying or if you have any questions, please contact Damian Albera at d.albera@proclinical.com

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.