Medical and Regulatory Affairs - Cell Therapy Medical Communication Specialist
Spectraforce Technologies
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
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
Vacancy posted 12 hours ago
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