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Translational Medicine Program Manager - Princeton New Jersey
Company: Disability Solutions Location: Princeton, New Jersey
Posted On: 05/04/2024
Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.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. Read more: careers.bms.com/working-with-us .Bristol-Myers Squibb is actively conducting translational medicine research to further our understanding of cancer biology and to identify which patient populations may be more likely to derive benefit from Immuno-Oncology (I-O). Bristol-Myers Squibb has long believed the future of cancer research is dependent on investments in science and partnerships. Collaboration is integrated into our organizational framework across translational medicine and R&D.The Solid Tumor Translational Medicine Team is responsible for program and project support for strategic and tactical planning and management of biomarker, bioanalytical and translational activities that contribute to asset development and platform technology advancement. The organization has accountability for broad, translational compliance and quality activities, as well as non-GxP lab-based quality and compliance. We have an exciting new opportunity in Program Management for the Translational Medicine Leader in support of the Solid Tumor portfolio, driving the development and facilitation of the broad, integrated plans to enable the delivery of the translational medicine portfolio.Position Responsibilities - Integral partnering with translational team(s) to develop and evolve translational strategies and the tactical project plans to achieve the strategic goals of the team.
- Partners with clinical operational planning to align on timelines and details necessary to inform clinical progress, major activities include: protocol design, rapid data acquisition, specimen collection, selection, routing, testing, and ingestion/analysis/reporting of analytical results.
- Identification, documentation and management of issues and risks, together with mitigation strategies for the portfolio of assets managed by the translational Leader
- Primary scope includes: Internal scientific partnerships driving biomarker sub-studies, translational R&D efforts and bioinformatics approaches to scientific evaluation of critical hypotheses, external collaborations for data acquisition, analysis and study activities, publications and presentations (internal and external), and regulatory responses and interactions.
- Establishing communication channels and meeting agendas to drive translational portfolio delivery and documenting outcomes, decisions and key learnings to enhance collaboration and communication.
- Driving biomarker analysis and activities, including but not limited to, facilitating data transfer specification creation in collaboration with technical leads, and coordination with both internal and external partners to support biomarker sample movement - as needed.
- Creating visibility and maintaining transparency into collaborative activity that contributes to the translational plan for the key questions.
- Elaborating and ensuring effective execution of a robust process for regular program and portfolio strategy reviews facilitated by scientific translational staff.
- Serving as PM Lead to support strategic and process improvement initiatives affecting his/her portfolio area(s) as required.Basic Qualifications
- Bachelor's degree with a minimum 4-6 years of pharma or medical device experience, 2-4 years project management experience or equivalent; PMP certification desirable.
- Strong project management skills, outcomes oriented, and results driven
- Demonstrates effective communication skills, cross-functional collaboration skills, and cross-cultural awareness
- Works with a high level of independence to lead projects and teams, reaches out to manager for expertise and support (as needed).
- Good Understanding of organizational, analytical, and planning skills
- Effectively utilizes project management tools and information technology systems such as Microsoft Office, Project, Excel, Visio, Spotfire, etc.Preferred Qualifications
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