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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 |
Working with Us
- 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
- 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
- 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
- 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
- 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
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