Medical Science Liaison Immunology - Admilparant (NC)
Bristol Myers Squibb
2 months ago
On-site
Raleigh, NC
Medical Affairs
Position: Medical Science Liaison, Immunology (Field - NC)
Key Responsibilities
- Develop and maintain relationships with academic/community research thought leaders, appropriate HCPs, and access stakeholders within a defined geography to answer scientific, unsolicited product, and HEOR questions.
- Use various interaction channels (1:1, group presentations, remote, etc.); demonstrate proficiency with scientific resources and presentations.
- Present information effectively to thought leaders/HCPs and respond to questions with medical accuracy and compliance with local procedures, ethical/legal guidelines.
- Assess the medical landscape by meeting with thought leaders/HCPs/access stakeholders to understand needs and expertise.
- Continuously update knowledge on treatment strategies, products, unmet medical needs, clinical trials, and health economics outcomes research.
- Understand the competitive landscape and evolving healthcare models to address customer informational needs.
- Identify opportunities to partner with HCPs on disease-state initiatives, collaborative research, and ISR aligned with BMS strategy.
- Attend medical congresses and local/regional meetings.
- Collect and communicate meaningful medical insights to medical and commercial organizations.
- Develop geography-specific Field Medical and TL Interaction plans; contribute to cross-functional institution/account plans; develop/deliver scientifically meaningful medical programs.
- Establish customer-centric, compliant collaboration with cross-matrix field teams; support medical/scientific training and provide scientific updates to internal stakeholders.
- Provide scientific support at promotional meetings; evaluate speakers and support BMS-contracted speakers (if applicable).
- Support interventional and non-interventional research (e.g., identify/assess study sites) to facilitate patient recruitment and safe/effective use of investigational products.
- Provide recommendations/insights to clinical development on study/site feasibility; support HCPs with ISR submission/execution and study follow-up.
- Ensure pharmacovigilance documents are understood/applied by local investigators; alert appropriate BMS personnel to adverse events.
- Actively support CRO-sponsored studies.
Position Requirements / Qualifications
- MD, PharmD, PhD, APP, PA, or NP with experience in a specific disease area or broad medical background and relevant pharmaceutical experience.
- Disease area knowledge and understanding of scientific publications.
- Knowledge of scientific/clinical area, competitive landscape, and patient treatment trends.
- Knowledge of clinical trial design and process.
- Knowledge of national healthcare/access environment.
- Knowledge of HEOR core concepts.
- Excellent English language skills (spoken and written).
Experience Desired
- Minimum of 2 years in a clinical and/or pharmaceutical environment.
- Prior MSL experience.
- Ability to work independently and as a team player.
- Ability to translate scientific/clinical data for physicians to better serve patients.
- Strong communication and presentation skills.
- Ability to build peer-to-peer relationships.
- Ability to quickly learn new subject areas and environments.
Essential Qualification
- Ability to drive a company-provided car; responsible and safe driving history and ethics/integrity.
Travel Requirement
- Travel required; field-based role—live in the territory managed or within 50 miles of its borders; spend majority of time in the field.
Compensation (if applicable)
- Field - United States: $166,090 - $201,262 (full-time FTE basis). Additional incentive opportunities may be available.
Benefits (explicitly listed)
- Health Coverage (medical, pharmacy, dental, vision); Wellbeing Support programs (e.g., EAP); Financial Well-being/Protection (401(k), disability, life insurance, etc.); Paid Time Off (including flexible time off/holiday details as stated).
Application Instructions
- Apply for the role even if the resume does not perfectly align with requirements.
Key Responsibilities
- Develop and maintain relationships with academic/community research thought leaders, appropriate HCPs, and access stakeholders within a defined geography to answer scientific, unsolicited product, and HEOR questions.
- Use various interaction channels (1:1, group presentations, remote, etc.); demonstrate proficiency with scientific resources and presentations.
- Present information effectively to thought leaders/HCPs and respond to questions with medical accuracy and compliance with local procedures, ethical/legal guidelines.
- Assess the medical landscape by meeting with thought leaders/HCPs/access stakeholders to understand needs and expertise.
- Continuously update knowledge on treatment strategies, products, unmet medical needs, clinical trials, and health economics outcomes research.
- Understand the competitive landscape and evolving healthcare models to address customer informational needs.
- Identify opportunities to partner with HCPs on disease-state initiatives, collaborative research, and ISR aligned with BMS strategy.
- Attend medical congresses and local/regional meetings.
- Collect and communicate meaningful medical insights to medical and commercial organizations.
- Develop geography-specific Field Medical and TL Interaction plans; contribute to cross-functional institution/account plans; develop/deliver scientifically meaningful medical programs.
- Establish customer-centric, compliant collaboration with cross-matrix field teams; support medical/scientific training and provide scientific updates to internal stakeholders.
- Provide scientific support at promotional meetings; evaluate speakers and support BMS-contracted speakers (if applicable).
- Support interventional and non-interventional research (e.g., identify/assess study sites) to facilitate patient recruitment and safe/effective use of investigational products.
- Provide recommendations/insights to clinical development on study/site feasibility; support HCPs with ISR submission/execution and study follow-up.
- Ensure pharmacovigilance documents are understood/applied by local investigators; alert appropriate BMS personnel to adverse events.
- Actively support CRO-sponsored studies.
Position Requirements / Qualifications
- MD, PharmD, PhD, APP, PA, or NP with experience in a specific disease area or broad medical background and relevant pharmaceutical experience.
- Disease area knowledge and understanding of scientific publications.
- Knowledge of scientific/clinical area, competitive landscape, and patient treatment trends.
- Knowledge of clinical trial design and process.
- Knowledge of national healthcare/access environment.
- Knowledge of HEOR core concepts.
- Excellent English language skills (spoken and written).
Experience Desired
- Minimum of 2 years in a clinical and/or pharmaceutical environment.
- Prior MSL experience.
- Ability to work independently and as a team player.
- Ability to translate scientific/clinical data for physicians to better serve patients.
- Strong communication and presentation skills.
- Ability to build peer-to-peer relationships.
- Ability to quickly learn new subject areas and environments.
Essential Qualification
- Ability to drive a company-provided car; responsible and safe driving history and ethics/integrity.
Travel Requirement
- Travel required; field-based role—live in the territory managed or within 50 miles of its borders; spend majority of time in the field.
Compensation (if applicable)
- Field - United States: $166,090 - $201,262 (full-time FTE basis). Additional incentive opportunities may be available.
Benefits (explicitly listed)
- Health Coverage (medical, pharmacy, dental, vision); Wellbeing Support programs (e.g., EAP); Financial Well-being/Protection (401(k), disability, life insurance, etc.); Paid Time Off (including flexible time off/holiday details as stated).
Application Instructions
- Apply for the role even if the resume does not perfectly align with requirements.