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Job Details


Bristol-Meyers Squibb, Co.

Senior Manager, Trial Supplies Management (R1554481-en-us)

Pharmaceuticals

All

Yearly

No

Princeton, New Jersey, United States

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

The Drug Supply Manager manages a small team within Drug Supply Management to support the clinical supply needs of several projects, normally within the same therapeutic area.

Responsibilities will include:

  • Manages the drug supply component of the Drug Development Plan (including forecasting for manufacturing/procurement, packaging/labeling, and distribution) required for drug program and corresponding protocols and updating plan as required for changes to enrollment/projected treatment duration.
  • Provides Clinical Supply Operations the program specific manufacturing and packaging requests, and prioritizes the associated work.
  • Advises Clinical Supply Operations (CSO) and Clinical management of resource constraints and recommends strategies which will influence the ability of CSO to meet existing or anticipated demands.
  • Coordinates with Operations Lead on the Full Development Team to ensure timely delivery of quality clinical supplies to support clinical programs and protocols.
  • Creates close collaborations to meet key milestones in the clinical supply process including: decisions on clinical supply strategies and designs, delivery of comparators and approved documentation to support clinical supply production.
  • Manages clinical supply budget.
  • Sets strategic direction for drug supply outsourcing needs and nurtures relationships to make outsourcing options available.
  • In collaboration with Randomization Manager, manages IVRS development activities.
  • Develops and maintains effective interfaces with key customers (external and internal). Fully understands the clinical study and clinical supply processes; viewed by peers as a leader with a high level of respectability and complete knowledge of processes and strategies.
  • Demonstrates leadership skills by driving for continuous improvement and encouraging and supporting collaboration across departments.
  • Demonstrates a strong consistent display of team behavior by actively participating in project-related teams and is accountable for supply related component.
  • Has a high level of problem solving skills and uses them to monitor key milestones in the global clinical supply process.
  • Recommends and implements ways to improve the efficiency of clinical supply processes.

Qualified Candidates:

  • Bachelor’s degree in Pharmacy or related science with 5-10 years of experience in the pharmaceutical industry with a focus in clinical supplies.
  • Strong understanding of the drug supply, distribution and packaging process.
  • Demonstrated ability to work with and manage people/teams in a culturally diverse, complex, changing environment for the timely delivery of clinical supplies.
  • Ability to effectively communicate and persuade others to accomplish clinical supply goals and objectives.
  • Proven ability to develop others through leading by example.
  • Ability to forecast and allocate resources to manage clinical supply programs with focus on meeting the program objectives.
  • Be able to apply Research and Development operating philosophy and operate within policies and procedures.
  • Must have strong problem solving skills, broad computer program literacy, including MS Word and Excel.
  • Excellent knowledge of the global clinical supply and clinical study processes, of cGMP and GCP regulations, ICH Guidelines as it relates to Good Distribution Practices (GDPs) and local country drug shipment regulations.
  • Project planning skills to make optimum use of resources and to meet timelines. Effective communication and knowledge of how to impact and influence people.
  • Excellent interpersonal skills. Self-motivated with a proven ability to organize project activity to meet multiple project timelines.

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.

To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to . Visit[Register to View] target="_blank"> [Register to View] to access our complete Equal Employment Opportunity statement.

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