Bristol-Myers Squibb
Clinical Development Program Lead, Neuropsychiatry (Executive Director)
Bristol-Myers Squibb, San Diego, California, United States, 92189
Clinical Development Program Lead, Neuropsychiatry (Executive Director)
Join Bristol Myers Squibb as a
Clinical Development Program Lead, Neuropsychiatry (Executive Director) . This role involves leading clinical development strategies, supervising teams, and collaborating across functions to advance neuropsychiatry projects. The position reports to the Head of Clinical Development and is a key member of the executive leadership team. Position Summary : The Clinical Development Program Leader oversees the design and execution of clinical trials, manages teams of clinical professionals, and contributes to strategic planning and regulatory submissions. Key Responsibilities : Include setting clinical strategies, supervising trial development, stakeholder engagement, governance participation, and supporting lifecycle management of programs. Qualifications & Experience : MD or equivalent, with over 10 years of clinical trial and drug development experience, including management and regulatory expertise. Experience in neuropsychiatry and global clinical research is preferred. Additional Details : The role requires domestic and international travel, offers competitive compensation, and benefits aligned with industry standards. The work environment emphasizes diversity, inclusion, and work-life balance. Note : This job posting is active and not expired.
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Join Bristol Myers Squibb as a
Clinical Development Program Lead, Neuropsychiatry (Executive Director) . This role involves leading clinical development strategies, supervising teams, and collaborating across functions to advance neuropsychiatry projects. The position reports to the Head of Clinical Development and is a key member of the executive leadership team. Position Summary : The Clinical Development Program Leader oversees the design and execution of clinical trials, manages teams of clinical professionals, and contributes to strategic planning and regulatory submissions. Key Responsibilities : Include setting clinical strategies, supervising trial development, stakeholder engagement, governance participation, and supporting lifecycle management of programs. Qualifications & Experience : MD or equivalent, with over 10 years of clinical trial and drug development experience, including management and regulatory expertise. Experience in neuropsychiatry and global clinical research is preferred. Additional Details : The role requires domestic and international travel, offers competitive compensation, and benefits aligned with industry standards. The work environment emphasizes diversity, inclusion, and work-life balance. Note : This job posting is active and not expired.
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