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Job Title


Cell Therapy Medical Communication Specialist


Company : Artech LLC


Location : Lawrence Township, NJ


Created : 2026-04-19


Job Type : Full Time


Job Description

Job Title: Cell Therapy Medical Communication Specialist Location: 50% onsite at Princeton Pike or Giralda Farms Duration: 12 Months Pay Rate: $77.58 Top Requirements: • 5-10 years of Pharmaceutical/Healthcare industry experience with a focus on medical communications; experience in both local country & global preferred • Advance scientific degree, PharmD, PhD or MD preferred • Working knowledge of Client suite of applications, and familiar with publication management (iEnvision) and content management (Veeva) tools • Ability to manage timelines and quality of work using strong organizational, communication, facilitation and interpersonal skills 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 Client internal audiences related to communication landscape, HCP preferences, publication and scientific content planning, data disclosure / dissemination. • Ensure Client 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 Client suite of applications, and familiar with publication management (iEnvision) and content management (Veeva) tools