Medical Science Liaison, Camzyos (E. MA, ME, NH)
Bristol Myers Squibb
6 days ago
On-site
Lawrence, NJ
Medical Affairs
Position Requirements:
- MD, PharmD, PhD, APP, PA, NP with experience in a specific Disease Area or with a broad medical background and relevant pharmaceutical experience.
- Disease area knowledge and understanding of scientific publications.
- Knowledge of a scientific/clinical area, competitive landscape, and patient treatment trends.
- Knowledge of clinical trial design and process.
- Knowledge of the national healthcare and access environment.
- Knowledge of HEOR core concepts.
- Excellent English (spoken and written).
Key Responsibilities:
- Develop and maintain relationships with academic/community research thought leaders, appropriate HCPs, and access stakeholders in a defined geography to answer scientific, unsolicited product, and HEOR questions.
- Use multiple channels (1:1, group presentations, remote) to present and discuss scientific information; respond to questions with medical accuracy and compliance.
- Assess the medical landscape by meeting with thought leaders/HCPs/access stakeholders; continuously update knowledge on treatment strategies, products, unmet needs, clinical trials, and HEOR.
- Understand competitive landscape and prepare to address customer informational needs.
- Identify opportunities to partner on disease-state initiatives, collaborative research, and ISR aligned with company objectives.
- Attend medical congresses and local/regional meetings; collect and communicate meaningful medical insights to support strategy and decisions.
- Develop geography-specific field medical/TL interaction plans and contribute to institution/account planning and medical programs/projects.
- Establish compliant, customer-centric collaboration with cross-matrix field teams; provide product/scientific training and updates to internal stakeholders.
- Support clinical trial activities (interventional and non-interventional): site identification/feasibility, ISR support, pharmacovigilance procedural adherence and adverse event escalation, and support CRO-sponsored studies.
Experience Desired:
- Minimum 2 years working in a clinical and/or pharmaceutical environment.
- Prior MSL experience.
- Ability to work independently and as a team player.
- Ability to translate data for physicians; strong communication/presentation skills; develop peer-to-peer relationships; rapid learning; demonstrate company values.
Essential Qualifications & Travel:
- Ability to drive a company-provided car; safe, ethical driving history.
- Travel required; field-based; live in territory or within 50 miles of territory borders.
Benefits (explicitly stated):
- Health Coverage (medical, pharmacy, dental, vision); Wellbeing Support; 401(k) and insurance/disability protections.
- Work-life benefits include Paid Time Off (flexible time off or vacation/hours depending on location/employee type) and potential additional time off based on eligibility.
Compensation (explicitly stated):
- $166,090–$201,262 (Field - United States).
- MD, PharmD, PhD, APP, PA, NP with experience in a specific Disease Area or with a broad medical background and relevant pharmaceutical experience.
- Disease area knowledge and understanding of scientific publications.
- Knowledge of a scientific/clinical area, competitive landscape, and patient treatment trends.
- Knowledge of clinical trial design and process.
- Knowledge of the national healthcare and access environment.
- Knowledge of HEOR core concepts.
- Excellent English (spoken and written).
Key Responsibilities:
- Develop and maintain relationships with academic/community research thought leaders, appropriate HCPs, and access stakeholders in a defined geography to answer scientific, unsolicited product, and HEOR questions.
- Use multiple channels (1:1, group presentations, remote) to present and discuss scientific information; respond to questions with medical accuracy and compliance.
- Assess the medical landscape by meeting with thought leaders/HCPs/access stakeholders; continuously update knowledge on treatment strategies, products, unmet needs, clinical trials, and HEOR.
- Understand competitive landscape and prepare to address customer informational needs.
- Identify opportunities to partner on disease-state initiatives, collaborative research, and ISR aligned with company objectives.
- Attend medical congresses and local/regional meetings; collect and communicate meaningful medical insights to support strategy and decisions.
- Develop geography-specific field medical/TL interaction plans and contribute to institution/account planning and medical programs/projects.
- Establish compliant, customer-centric collaboration with cross-matrix field teams; provide product/scientific training and updates to internal stakeholders.
- Support clinical trial activities (interventional and non-interventional): site identification/feasibility, ISR support, pharmacovigilance procedural adherence and adverse event escalation, and support CRO-sponsored studies.
Experience Desired:
- Minimum 2 years working in a clinical and/or pharmaceutical environment.
- Prior MSL experience.
- Ability to work independently and as a team player.
- Ability to translate data for physicians; strong communication/presentation skills; develop peer-to-peer relationships; rapid learning; demonstrate company values.
Essential Qualifications & Travel:
- Ability to drive a company-provided car; safe, ethical driving history.
- Travel required; field-based; live in territory or within 50 miles of territory borders.
Benefits (explicitly stated):
- Health Coverage (medical, pharmacy, dental, vision); Wellbeing Support; 401(k) and insurance/disability protections.
- Work-life benefits include Paid Time Off (flexible time off or vacation/hours depending on location/employee type) and potential additional time off based on eligibility.
Compensation (explicitly stated):
- $166,090–$201,262 (Field - United States).