Medical Science Liaison - Cardiovascular (Houston, South Texas & Louisiana)
Bristol Myers Squibb
June 27, 2026
On-site
Houston, TX
Medical Affairs
Position: Medical Science Liaison, Cardiovascular (Houston, South Texas & Louisiana)
Responsibilities
- Identify disease and product-related medical needs in a defined geography; serve as a medical resource for external stakeholders.
- Develop and maintain relationships with Thought Leaders (TLs) and Healthcare Providers (HCPs) to drive meaningful scientific exchange.
- Answer scientific, unsolicited product, and HEOR-related questions via 1:1, group presentations, remote, etc.
- Use scientific resources to present accurate information and respond to questions per ethical/legal guidelines.
- Assess the medical landscape; continuously update knowledge (treatment strategies, products, unmet needs, clinical trials, HEOR).
- Partner with HCPs on disease-state initiatives, collaborative research, and investigator-sponsored research (ISR) aligned with BMS objectives.
- Attend medical congresses/meetings; collect and communicate medical insights to support strategy and business decisions.
- Develop geography-specific field/TL interaction plans; contribute to institution/account planning and local medical programs.
- Establish customer-centric, compliant collaboration with cross-matrix field teams; support medical/product training and internal scientific updates.
- Provide scientific support at promotional meetings; evaluate speakers/support contracted speakers (if applicable).
- Support clinical trial activities: identify potential study sites; recommend feasibility; support ISR submission/execution; ensure pharmacovigilance procedures and escalate adverse events; support CRO-sponsored studies.
Required Experience/Qualifications
- MD, PharmD, PhD, APP, PA, or NP with experience in a disease area or broad medical background and relevant pharmaceutical experience.
- Ability to drive a company-provided car (safe, ethical driving history) and travel within the territory.
Knowledge/Skills Desired
- Disease area and scientific publication understanding; clinical trial design/process knowledge.
- Knowledge of competitive landscape, patient treatment trends, national healthcare/access environment, and HEOR concepts.
- Excellent English (spoken/written); strong communication and presentation skills.
Experience Desired
- Minimum 2 years in clinical and/or pharmaceutical environment; prior MSL experience preferred.
- Ability to work independently, translate data for physicians, build peer-to-peer relationships, and quickly learn new subject areas.
Travel Requirement
- Field-based; live in the territory or within 50 miles of territory borders; majority of time in the field.
Compensation/Bens (as stated)
- Field (US): $166,090–$201,262; additional incentive cash/stock may be available (eligibility-based).
Application instruction
- Apply for the role (if resume doesn’t perfectly match, apply anyway).
Responsibilities
- Identify disease and product-related medical needs in a defined geography; serve as a medical resource for external stakeholders.
- Develop and maintain relationships with Thought Leaders (TLs) and Healthcare Providers (HCPs) to drive meaningful scientific exchange.
- Answer scientific, unsolicited product, and HEOR-related questions via 1:1, group presentations, remote, etc.
- Use scientific resources to present accurate information and respond to questions per ethical/legal guidelines.
- Assess the medical landscape; continuously update knowledge (treatment strategies, products, unmet needs, clinical trials, HEOR).
- Partner with HCPs on disease-state initiatives, collaborative research, and investigator-sponsored research (ISR) aligned with BMS objectives.
- Attend medical congresses/meetings; collect and communicate medical insights to support strategy and business decisions.
- Develop geography-specific field/TL interaction plans; contribute to institution/account planning and local medical programs.
- Establish customer-centric, compliant collaboration with cross-matrix field teams; support medical/product training and internal scientific updates.
- Provide scientific support at promotional meetings; evaluate speakers/support contracted speakers (if applicable).
- Support clinical trial activities: identify potential study sites; recommend feasibility; support ISR submission/execution; ensure pharmacovigilance procedures and escalate adverse events; support CRO-sponsored studies.
Required Experience/Qualifications
- MD, PharmD, PhD, APP, PA, or NP with experience in a disease area or broad medical background and relevant pharmaceutical experience.
- Ability to drive a company-provided car (safe, ethical driving history) and travel within the territory.
Knowledge/Skills Desired
- Disease area and scientific publication understanding; clinical trial design/process knowledge.
- Knowledge of competitive landscape, patient treatment trends, national healthcare/access environment, and HEOR concepts.
- Excellent English (spoken/written); strong communication and presentation skills.
Experience Desired
- Minimum 2 years in clinical and/or pharmaceutical environment; prior MSL experience preferred.
- Ability to work independently, translate data for physicians, build peer-to-peer relationships, and quickly learn new subject areas.
Travel Requirement
- Field-based; live in the territory or within 50 miles of territory borders; majority of time in the field.
Compensation/Bens (as stated)
- Field (US): $166,090–$201,262; additional incentive cash/stock may be available (eligibility-based).
Application instruction
- Apply for the role (if resume doesn’t perfectly match, apply anyway).