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Medical Science Liaison Immunology - Jacksonville, FL

Remote / Online - Candidates ideally in
Jacksonville, Duval County, Florida, 32290, USA
Listing for: VetJobs
Remote/Work from Home position
Listed on 2026-07-18
Job specializations:
  • Healthcare
    Medical Science Liaison, Clinical Research
Salary/Wage Range or Industry Benchmark: 166090 - 201262 USD Yearly USD 166090.00 201262.00 YEAR
Job Description & How to Apply Below

Job Title

Medical Science Liaison, Immunology - Admilparant

Location

Field - N. FL, S. GA

Overview

Our organization works with partner companies to source qualified talent for open roles. This position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors and their Caregivers. Our work transforms patient lives and careers of those who do it, offering opportunities uncommon in scale and scope. We value balance and flexibility and provide competitive benefits, services and programs that support employees’ personal and professional goals.

Key Responsibilities
  • Develop and maintain relationships with academic and community research thought leaders, appropriate healthcare providers (HCPs) and access stakeholders within a defined geography.
  • Use various interaction channels – one‑on‑one, group presentations, remote meetings, etc. – to deliver scientific information.
  • Demonstrate proficiency in using available scientific resources and presentations.
  • Present scientific information to TLs/HCPs and respond to questions while ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines.
  • Assess the medical landscape by meeting with TLs/HCPs/Access stakeholders to understand their needs and expertise.
  • Continuously update own knowledge on treatment strategies, products, unmet medical needs, clinical trials, health economics outcomes research (HEOR) and scientific activities.
  • Understand the competitive landscape and evolving healthcare models, and actively prepare to address informational needs of customers.
  • Identify opportunities to partner with HCPs on disease‑state initiatives, collaborative research projects and investigator‑sponsored research (ISR) that align with BMS strategic objectives.
  • Attend medical congresses and local/regional meetings.
  • Collect and provide meaningful medical insights and/or impact by communicating these back to the medical and commercial organizations to support strategy development and business decisions.
  • Contribute to the Medical Plan by developing geography‑specific field medical and TL interaction plans based on therapeutic area objectives and TL needs.
  • Adopt institution/account planning approach and contribute to cross‑functional institution/account plans.
  • Provide medical support by establishing a customer‑centric, compliant collaboration with cross‑matrix field teams within the assigned geography.
  • Support initial and ongoing medical/scientific area and product‑specific training, and provide key scientific updates to internal stakeholders (Commercial, Regulatory, Pharmacovigilance, Legal, HEOR, Value Access & Payment).
  • Present scientific and clinical data at promotional meetings, evaluate speakers and provide support to BMS‑contracted speakers.
  • Participate in assigned congress activities.
  • Support interventional and non‑interventional research studies (e.g., identification and assessment of potential study sites) to facilitate patient recruitment and discuss the safe and effective use of BMS investigational products.
  • Provide recommendations and insights to clinical development teams on study and site feasibility based on knowledge of the field and direct contacts with potential investigators.
  • Support HCPs with ISR submission, execution process and study follow‑up as agreed upon with home office medical and Global Development Operations (GDO).
  • Ensure BMS pharmacovigilance procedural documents are understood and applied by investigators of local studies and alert appropriate BMS personnel to identified adverse events.
  • Actively support CRO‑sponsored studies as defined by the study scope document.
Qualifications
  • Minimum education:

    Ph.D. (MD, PharmD, PhD, APP, PA, NP acceptable with disease‑area experience).
  • Experience:

    Minimum 2 years working in a clinical and/or pharmaceutical environment.
  • Prior MSL experience desirable.
  • Knowledge of a specific disease area or broad medical background with pharmaceutical experience.
  • Understanding of scientific publications, clinical trial design and process, national healthcare and access environment, and HEOR core concepts.
  • Excellent English language skills, spoken and written.
  • Str…
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