Medical and Regulatory Affairs - Cell Therapy Medical Communication Specialist
Spectraforce Technologies, Lawrenceville, NJ, United States
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
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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
#J-18808-Ljbffr