Clinical Program Management Lead

2 weeks ago

New Brunswick, New Jersey, United States Bristol-Myers Squibb Full time
Join Our Team
At Bristol Myers Squibb, we offer a unique opportunity to engage in work that is both challenging and impactful. Our environment fosters innovation and collaboration, allowing you to contribute to transformative projects that enhance the lives of patients and advance your career.

Role Overview:
The Clinical Program Management Lead plays a crucial role in overseeing the planning and execution of designated clinical studies within the RayzeBio initiatives. This position involves managing the Clinical Research Organization (CRO) and associated vendors, ensuring compliance with established corporate protocols, Good Clinical Practice (GCP), and relevant regulatory guidelines. The goal is to meet project objectives within specified timelines and budget constraints. You will collaborate closely with the Senior Director of Clinical Program Management and fellow Clinical Program Managers to ensure the successful delivery of all clinical studies.

Key Responsibilities:
  • Facilitates the evaluation of study plans and documentation, including informed consent forms and monitoring strategies.
  • Assists in the oversight of CROs to guarantee timely and budget-compliant study completion, adhering to all regulatory standards.
  • Manages selected study vendors, reviewing operational plans and performance metrics, while identifying and mitigating risks.
  • Actively participates in meetings with CROs and vendors to ensure effective study execution.
  • Supports the planning and maintenance of study timelines, ensuring the project team remains aligned with deliverables.
  • Monitors and reports on study progress, managing budgets and invoicing in accordance with contracts.
  • Summarizes vendor performance data and escalates risks to the Clinical Operations Program Lead as necessary.
  • Willingness to travel up to 20% as required.
Qualifications:
  • Bachelor's degree in a relevant field.
  • A minimum of 6 years of experience in Clinical Operations.
Skills:
  • Strong communication skills with a proactive approach.
  • Detail-oriented and organized, with a commitment to quality.
  • Ability to work effectively in cross-functional teams.
  • Adaptability to dynamic environments.
  • Proficiency in Microsoft Project and Smartsheets is preferred.
Physical Requirements:
Regular tasks include sitting, reaching, and effective communication. The role may require lifting up to 15 pounds occasionally.

Work Environment:
The work environment typically has a moderate noise level.

Commitment to Diversity:
Bristol Myers Squibb is dedicated to fostering an inclusive culture that values diverse perspectives. We encourage individuals from all backgrounds to apply and contribute to our mission of transforming patients' lives through science.

Health and Safety:
We prioritize the health and safety of our employees and recommend that all staff members stay updated with vaccinations, including Covid-19.

Data Privacy:
All personal data processed during the application process will be handled in accordance with applicable privacy regulations.

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