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Associate Director, Oncology Portfolio Early Assets And Cross-Tumor Biomarkers Medical Communications

Company

Bristol Myers Squibb

Address New Jersey, United States
Employment type PART_TIME
Salary
Category Pharmaceutical Manufacturing
Expires 2023-06-21
Posted at 11 months ago
Job Description
Working with Us


Challenging. 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


Position Summary


Position is an individual contributor who reports to the Director of Oncology Portfolio, Early Assets, and Biomarkers Medical Communications within the Medical Communications organization under Scientific Communications & Engagement, which is part of Global Medical Affairs, and is responsible for the strategy and execution of medical communication plans within the therapeutic area and asset/indication, worldwide (WW) and in the US market. The Early Assets and Cross-tumor Biomarkers Medical Communications lead will ensure communications for scientific exchange (publications and scientific content) related to the science and/or health economic value of BMS products and research data to inform healthcare providers (HCPs), patients, and payers in accordance with local regulations.


Key Responsibilities


A core member of the Oncology Medical Communications team, the Associate Director of Early Assets and Cross-tumor Biomarkers for WW/US Medical Communications, with a primary focus on publications, is accountable for the following


Medical Communications Strategy


  • Drive integrated scientific communications planning to establish a clear, viable, and compelling strategy for medical communications for assigned asset(s)/indication(s) within the therapeutic and disease area, aligned with overall Medical vision, strategy, and objectives
  • Lead and support as needed the development and execution of functionally integrated and aligned medical communications plans to ensure timely, high-quality journal submissions, publications, congress presentations, and delivery of internal and external scientific content; adjust communications plans in accordance with clinical trial results/milestones and changes in the healthcare landscape and in alignment with WW Medical and US Medical market-level strategy
  • Understand the communication needs across the therapeutic area and disease area that incorporate and align with enterprise-level strategies for the development and execution of functionally integrated publication plans and scientific content plans, with application and pull-through to Scientific Communication Platforms and Scientific Narratives
  • Project strong business acumen and ability to interface with matrix partners to prioritize tactics within Medical Communications budget targets and work within allocated resources


Data Dissemination


  • Provide expert scientific guidance, subject-matter expertise, and support to cross-functional BMS internal audiences related to the scientific communication landscape in the therapeutic and disease area, HCP preferences, publication and scientific content planning, data disclosure/dissemination, and represent BMS scientific communications to external investigators, key authors, and journal editors
  • Demonstrate scientific/research expertise to support the establishment of strong working collaborations with both internal and external disease-area experts to ensure quality data analysis, interpretation, communication planning, and data disclosure/dissemination
  • Promote and reinforce principles among authors and internal publication stakeholder community, ensuring publications are authored, written, and reviewed according to publication best practices and BMS standards and policies and for ensuring BMS publication & scientific content standards are aligned with Good Publication Practices and industry standards, and all BMS employees engaged in publication activities follow Good Publication Practices guidance with the highest degree of integrity, quality and transparency


Stakeholder Engagement


  • Participate in Medical Communications and Scientific Communications & Engagement organizational workstreams, taking a leadership role to help drive outcomes
  • Partner externally with third-party vendors to ensure the appropriate balance of internal and external execution of work
  • Function as a high-performing partner, externally and internally, emphasizing teamwork, cooperation, personal accountability, and a commitment to quality; model BMS behaviors and reinforce such behaviors at all levels in the organization
  • Ensure endorsement of scientific communications plans by relevant governance bodies prior to execution
  • Partner with Early Assets and Cross-tumor Biomarkers Medical Communications colleagues, WW/US Medical, HEOR colleagues, and other stakeholders to assess, plan, and allocate resources (budget, medical writing, biostatistical services) to ensure timely delivery of high-quality medical communications
  • Liaise with alliance/collaboration partners appropriately as required for select assets/indications in the TA
  • Enable and assist therapeutic area team with the collection and collation of clear metrics aligned to meeting customer needs and demonstrating desired outcomes and value of activities
  • Collaborate with internal stakeholders across the Medical matrix and other Scientific Communications & Engagement colleagues to leverage external insights that inform medical communications planning while ensuring efficiency and value
  • Assist Oncology Portfolio, Early Assets, and Biomarkers Team Lead/Director by acting as liaison/representative of Medical Communications at intra- and inter-departmental meetings, participating in decisions that impact the overall medical/scientific support of products within the therapeutic and asset teams
  • Demonstrate visible leadership by providing coaching and mentoring to colleagues on the team


Qualifications & Experience


  • Expertise across all aspects of scientific publication strategy, planning, and execution during all phases of drug development and commercialization process
  • Proven ability to think strategically at an enterprise level and lead teams to make strategic decisions even under conditions of ambiguity, evolving landscapes, and tight timelines
  • Ability to travel (domestically and internationally)
  • Ability to influence and negotiate appropriate solutions; ability to establish strong stakeholder relationships
  • Demonstrated success driving optimal business results in a large complex corporate environment with multiple priorities and tight timelines
  • Strong scientific knowledge of therapeutic and disease research areas, including HEOR, and familiarity with drug development and product lifecycle
  • Experience leading and executing across cross-functional, cross-cultural project teams, and collaborating across a stakeholder matrix, multiple markets, and global geographies
  • Advanced scientific degree, eg, PharmD, PhD, or MD preferred
  • Outstanding interpersonal, written, and verbal communication skills
  • Certified Medical Publication Professional (CMPP) and ISMPP active member highly desired
  • Adept at building credibility with external investigators and collaborative partners, evidenced by strong leadership behaviors and scientific excellence
  • Ability to manage timelines and quality of work using strong leadership, organizational, communication, facilitation, and interpersonal skills
  • A minimum of 4 years of pharmaceutical/healthcare industry experience with a focus on medical communications; experience in oncology is preferred
  • Ability to analyze and interpret trial data


Knowledge Desired


  • External compliance, transparency, and conflict-of-interest regulated work environments
  • Pharmaceutical/Healthcare Industry
  • Understanding of clinical trial design and execution, statistical methods, and clinical trial data reporting requirements
  • Working knowledge of Microsoft suite of applications, and familiar with publication management tool (DataVision)
  • In-depth knowledge of Good Publication Practices and guidance (GPP, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication


The starting compensation for this job is a range from $141,000 –$178,000, plus incentive cash and stock opportunities (based on eligibility).


The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed.


Final, individual compensation will be decided based on demonstrated experience.


Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Careers site.


Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.


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


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


COVID-19 Information


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.


BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.


BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.


Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.