Neurology Director jobs in Union, NJ

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The  Director, WW Medical Cell Therapy, Autoimmune, will report to a WW Medical Cell Therapy Autoimmune Lead, WW Medical Cell Therapy. The role is headquarters based and will provide scientific leadership and support for compounds in various stages of clinical development, as well as approved products within a therapeutic area.  This individual will support the design and implementation of  strategic disease area medical plans. When appropriate, they will also take a leadership role for the execution of BMS sponsored Medical Affairs trials, and assisting in the evaluation and support of collaborative and investigator-initiated trials.

The position holder represents Global Medical Affairs as needed on behalf of the Medical Cell Therapy Lead, serving as a therapeutic area expert in scientific, strategic and tactical discussions and presentations with internal colleagues, as well as with external experts and investigators. Represent WW Medical Cell Therapy at GPT/EDPT as a delegate of the Autoimmune Lead, provides input into  World-Wide Brand Team (WWBT) and supports country launches with strategic planning, in-house Medical and RML/MSL training, data dissemination, and creation of Integrated Evidence Plans (IEP) in conjunction with cross-functional team. He is responsible for the content and execution of Global Medical Affairs Advisory Boards.

Position Responsibilities

1.     Leadership responsibilities:  Strategic and Tactical

• Serve as the Medical and Scientific Expert for the Global Autoimmune Cellular Therapy  team and provide support for the Cellular Therapy Project Teams as needed

• Collaborate with and provide Medical content expertise in support of Global and Local Market Access and Marketing initiatives

• Collaborate with all Regional and Local Disease representatives and functional teams in Medical Affairs on Disease strategy and tactics

• Support/lead in the execution of Global advisory boards and steering committee meetings, but also be involved in assisting the regions on critical globally impactful advisory boards.

• Perform, as needed, research and analytics and provide recommendations to support quality medical decisions regarding clinical research, consultancy, and internal planning.

• Conduct research and provide directed analytics and valuable backgrounders, as well as provide recommendations and serve as Medical Leadership representative on Investigator Initiated Trials (ISRs) decisions. Provide review, recommendations, on new ISR and CR trials

• Serve as expert contributor on WWBT strategy in preparation for professional meetings, congresses, and local symposia

2.     Deliverable responsibilities:  Strategic and Tactical

• Partner with Scientific Communications on developing publication strategy, gap analysis, key messages in coordination with the Regions

• Lead the development of hypotheses and primary research in the generation of congress abstracts and publications to address unanswered questions and support Global and Local product launches

• Serve as reviewer for all Cellular Therapy  focused abstracts, presentations, and publications, as needed

• Identify educational opportunities and guide content generation and presentations to Global, Regional, and Local teams

• Help track budget for their own projects and provide guidance for execution of new statements of work

• High quality scientific/clinical content generation, input and review of (as needed):

  • Disease strategy/plans

  • Abstracts, posters, slides, manuscripts in disease area

  • Educational materials in disease area including slides, webcasts, etc.

  • Cooperative group proposals, study concepts, and IIT proposals and protocols in disease area

  • Key Opinion Leader (KOL) Steering committee meeting objectives, materials

  • Clinical Development Plans (CDPs), Commercial Brand Plans, Integrated Disease Plans

  • Lead the update and generation of IEPs in disease area and gain approval from Senior Leadership

  • Scientific educational grant requests

  • Patient advocacy grant requests in collaboration with the Advocacy team, serving as matter of expert

• Support the planning and execution of BMS Sponsored Trials, within appropriate standards for compliance, quality, timeliness, and budget

• Assist with scientific searches, data summaries, preparation for site visits/corporate visits/payor presentations

• Track priority Medical Affairs tactics and performance to goals/budget

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

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