Associate Director, Intercontinental Scientific
Vor 3 Tagen
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.
A core member of the Major Markets and Intercontinental Scientific Publications Team, the Associate Director for Intercontinental Scientific Publications is responsible for the planning and timely execution of scientifically accurate and strategically aligned publications that support the local medical communication needs of the Intercontinental Markets.
**Key Responsibilities**
- Leads across the BMS matrix to develop strategically aligned publication plans, congress submissions & presentations, and manuscripts in the Intercontinental Markets
- Ensures endorsement of publication plans by relevant governance bodies prior to execution, and continuously and continuously develops and maintains plans in conjunction with scientific landscape and in alignment with Local Market Medical, Worldwide (WW) Medical and WW Scientific Publications strategy
- Serves as the Intercontinental Market Publications point of contact between WW/Local Medical, WW Publications, and other matrix partners
- Provides publication management oversight to Local Market Medical
- Enhances bi-directional communication by understanding and sharing the WW publication plans to Local Market Medical and raises local publication needs to WW Medical/Publication teams, ensuring country/global level of awareness & connectivity
- Reviews publication drafts for scientific quality, and ensures alignment and consistency with author direction, the scientific communication platform, and scientific data
- Promotes and reinforces good publication practices and 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
- Identifies, selects, and manages third-party agencies and providers to ensure timely and compliant delivery of quality medical publications according to market publication plans
- Partners with WW Publication Leads and Market Medical to assess, plan, and allocate resources (budget, medical writing, biostatistical services) to ensure timely delivery of high-quality medical communications
- Facilitates decision making and escalates issues appropriately to ensure effective solutions and timely execution
- Demonstrates understanding of therapeutic disease areas, medical strategies, and objectives necessary to provide strategic input to a broad range of stakeholders for publication planning and data dissemination/disclosure
- Actively mentors and manages assigned direct report by ensuring the individual’s understanding and achievement of performance targets
- Supports growth and development of assigned direct report to prepare the individual for broader responsibilities
**Qualifications & Experience**
- 5+ years’ experience in Publications, preferably within Pharmaceutical/Healthcare Industry with focus on scientific publications
- Expertise across all aspects of scientific publication strategy, planning and execution during all phases of drug development and commercialization is strongly preferred
- Experience working in highly matrixed environment across a broad range of functional areas and effectively collaborating with the Medical Affairs, Health Outcomes, R&D, regulatory, legal, and commercial teams
- Understanding of clinical trial design and execution, statistical methods, and clinical trial data reporting requirements
- Outstanding interpersonal, written, and verbal communication skills with exceptional time management skills
- People management experience
- Ability to flexibly schedule and participate in teleconferences and virtual meetings across different time zones
- Ability to travel domestically and internationally
- Pharmaceutical/Healthcare Industry
- External compliance, transparency and conflict-of-interest regulated work environments
- In-depth knowledge of Good Publication Practices and guidance (GPP3, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication
- Understanding of clinical trial design and execution, statistical methods, and clinical trial data reporting requirements
- Cross-cultural/cross-geographical awareness and understanding
**#LI-Remote**
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 presen
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