Medical and Regulatory Affairs - Cell Therapy Medical Communication Specialist

Job Title:

Cell Therapy Medical Communication Specialist Onsite/Hybrid:

50% onsite at

Princeton Pike or Giralda Farms Duration:

12 Months Purpose and Scope of the

Position:

• Work with Medical Communication Director and the publications matrix team to help with development of publications and/or medical content within assigned therapeutic area

Required Competencies:

Knowledge, Skills, and Abilities:

• Advance scientific degree, PharmD, PhD or MD preferred
• 5-10 years of Pharmaceutical/Healthcare industry experience with a focus on medical communications; experience in both local country & global preferred
• Proven ability to work in an ambiguous environment with a focus on deliverables
• Ability to analyze and interpret trial data
• Ability to manage timelines and quality of work using strong organizational, communication, facilitation and interpersonal skills
• Ability to influence and negotiate appropriate solutions

Duties and Responsibilities:

• Take on assigned projects to help with development and execution of functionally integrated and aligned medical communications plans; adjust communications plans in accordance with clinical trial results/milestones and changes in the healthcare landscape
• Serve as a subject matter expert to BMS internal audiences related to communication landscape, HCP preferences, publication and scientific content planning, data disclosure / dissemination.
• Ensure BMS publication & scientific content standards are aligned with Good Publication Practices and industry standards to ensure the highest degree of integrity, quality and transparency

Education and Experience:

• Pharmaceutical/Healthcare Industry
• External compliance, transparency and conflict-of-interest regulated work environments
• 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
• Certified Medical Publication Professional (CMPP), and ISMPP active member highly desired
• 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 (iEnvision) and content management (Veeva) tools

Working Conditions:

Office/desk work in an open space environment