MSL/Sr. MSL Oncology, Multiple Myeloma (MI/OH/IN)
AbbVie
August 06, 2026
Remote friendly (Columbus, OH)
United States
$124,500 - $236,500 USD yearly
Medical Affairs
The MSL/Sr. MSL is a field-based scientific expert responsible for advancing scientific and medical understanding of AbbVie’s therapeutic areas through high-quality, non-promotional scientific exchange.
Responsibilities:
- Deliver high-quality, balanced, compliant scientific exchange with HCPs and scientific experts.
- Build and sustain credible, trust-based scientific relationships enabling two-way dialogue and Scientific Intelligence.
- Interpret and communicate therapeutic landscape data, disease state knowledge, and evolving standards of care.
- Generate, document, and share HCP perspectives and Scientific Intelligence to inform medical planning and evidence generation.
- Support evidence generation by raising clinical research awareness and engaging investigators where appropriate.
- Translate complex scientific/clinical information into clear, relevant discussions aligned to stakeholder needs.
- Collaborate with Medical Affairs/MHI, Clinical Development, Evidence Generation partners, and In-Field Team.
- Plan and execute scientific engagement aligned to medical objectives and territory priorities.
- Use approved tools/channels to optimize exchange while maintaining compliance.
- Ensure accurate, timely, compliant documentation.
Qualifications:
- Advanced scientific degree required (PharmD, PhD, MD, PA, NP, or equivalent).
- Experience in Medical Affairs, clinical research, academic science, or related scientific/healthcare roles.
- Evidence-based scientific discussion experience (ideally multiple myeloma).
- Foundational disease/mechanism/standards of care knowledge.
- Knowledge of clinical research principles, evidence types, and study design.
- Experience interpreting scientific literature/clinical trial data/RWE.
- Cross-functional medical/scientific collaboration experience.
Benefits (if applicable): paid time off; medical/dental/vision insurance; 401(k); long-term incentive eligibility.
Additional: Must live in the territory or be willing to self-relocate within the territory.
Responsibilities:
- Deliver high-quality, balanced, compliant scientific exchange with HCPs and scientific experts.
- Build and sustain credible, trust-based scientific relationships enabling two-way dialogue and Scientific Intelligence.
- Interpret and communicate therapeutic landscape data, disease state knowledge, and evolving standards of care.
- Generate, document, and share HCP perspectives and Scientific Intelligence to inform medical planning and evidence generation.
- Support evidence generation by raising clinical research awareness and engaging investigators where appropriate.
- Translate complex scientific/clinical information into clear, relevant discussions aligned to stakeholder needs.
- Collaborate with Medical Affairs/MHI, Clinical Development, Evidence Generation partners, and In-Field Team.
- Plan and execute scientific engagement aligned to medical objectives and territory priorities.
- Use approved tools/channels to optimize exchange while maintaining compliance.
- Ensure accurate, timely, compliant documentation.
Qualifications:
- Advanced scientific degree required (PharmD, PhD, MD, PA, NP, or equivalent).
- Experience in Medical Affairs, clinical research, academic science, or related scientific/healthcare roles.
- Evidence-based scientific discussion experience (ideally multiple myeloma).
- Foundational disease/mechanism/standards of care knowledge.
- Knowledge of clinical research principles, evidence types, and study design.
- Experience interpreting scientific literature/clinical trial data/RWE.
- Cross-functional medical/scientific collaboration experience.
Benefits (if applicable): paid time off; medical/dental/vision insurance; 401(k); long-term incentive eligibility.
Additional: Must live in the territory or be willing to self-relocate within the territory.