Opportunity Details

Medical Science Director
Posted: 07/15/2026
Client name: Client Name Text
Job Function: Technology
Source: Source Text
Location: Parsippany, New Jersey, United States
Posted: 07/15/2026
Description

The client is seeking a Medical Science Director/Medical Science Liaison to support medical affairs activities across oncology and related therapeutic areas such as infectious disease, nephrology, and acute care. In this role, you will support compliant scientific exchange by gathering insights and partnering cross-functionally to help shape medical strategies. You will serve as a scientific resource for healthcare providers, key opinion leaders, pharmacy stakeholders, and institutional decision-makers across both inpatient and outpatient healthcare settings.

You will identify, engage, and maintain relationships with emerging and established key opinion leaders within clinical decision-making institutions. Responsibilities will include developing scientific discussions for medical congresses, advisory boards, and professional society meetings, and contributing to publication planning and evidence dissemination through internal cross-functional support. You will also support clinical trial-related efforts such as site identification, investigator education, and collaborative research initiatives.

The ideal candidate will have an advanced healthcare or scientific degree (such as MD, DO, PharmD, PhD, DNP, NP, or PA-C, or an equivalent qualification). Oncology experience is required, with experience in infectious disease, nephrology, critical care, or supportive oncology strongly preferred. Additional experience in an academic institution, healthcare system, pharmaceutical, biotech, or related environment is preferred, along with strong scientific communication and presentation skills, the ability to operate independently while managing multiple priorities, and demonstrated proficiency in evaluating scientific literature, interpreting medical data, and gathering insights. You will also handle medical information requests, support document adverse events, and ensure adherence to pharmacovigilance procedures.

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