MSL/Sr. MSL Oncology, Multiple Myeloma (Pacific Northwest)
AbbVie
June 30, 2026
On-site
Seattle, WA
$124,500 - $236,500 USD yearly
Medical Affairs
The Medical Science Liaison (MSL) is a field-based scientific expert responsible for advancing scientific and medical understanding through high-quality, non-promotional scientific exchange. Builds trusted relationships with healthcare professionals and scientific experts, generates healthcare professional perspectives and Scientific Intelligence, and supports evidence generation.
Responsibilities:
- Deliver high-quality, balanced, compliant scientific exchange tailored to clinical context and informational needs.
- Build and sustain credible, trust-based relationships enabling meaningful two-way dialogue and Scientific Intelligence.
- Interpret and communicate AbbVie/therapeutic landscape data, disease state knowledge, and evolving standards of care with scientific rigor.
- Generate, document, and share healthcare professional perspectives and Scientific Intelligence to inform medical planning and evidence generation.
- Support evidence generation by raising scientific awareness of clinical research and engaging investigators.
- Translate complex scientific/clinical information into clear discussions aligned to stakeholder needs.
- Collaborate with Medical Affairs and Health Impact (MHI), Clinical Development, Evidence Generation partners, and the In-Field team (IFT).
- Plan and execute scientific engagement activities aligned to medical objectives and territory priorities.
- Use approved tools/channels/approaches to optimize exchange while maintaining full compliance.
- Ensure accurate, timely, compliant documentation per AbbVie policies and regulatory standards.
Qualifications:
- Advanced scientific degree required (PharmD, PhD, MD, PA, NP, or equivalent).
- Experience in Medical Affairs, clinical research, academic science, or other scientific/healthcare roles.
- Evidence-based scientific discussions with HCPs/scientific stakeholders (multiple myeloma preferred).
- Foundational disease/biologic/mechanism and standards of care knowledge.
- Working knowledge of clinical research principles, evidence types, and study design.
- Experience interpreting scientific literature/trial data/real-world evidence.
- Cross-functional collaboration experience.
- Travel up to 75%.
- Candidate must live in the territory or be willing to self-relocate within the territory.
Benefits (if eligible): paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k); eligible for long-term incentive programs.
Responsibilities:
- Deliver high-quality, balanced, compliant scientific exchange tailored to clinical context and informational needs.
- Build and sustain credible, trust-based relationships enabling meaningful two-way dialogue and Scientific Intelligence.
- Interpret and communicate AbbVie/therapeutic landscape data, disease state knowledge, and evolving standards of care with scientific rigor.
- Generate, document, and share healthcare professional perspectives and Scientific Intelligence to inform medical planning and evidence generation.
- Support evidence generation by raising scientific awareness of clinical research and engaging investigators.
- Translate complex scientific/clinical information into clear discussions aligned to stakeholder needs.
- Collaborate with Medical Affairs and Health Impact (MHI), Clinical Development, Evidence Generation partners, and the In-Field team (IFT).
- Plan and execute scientific engagement activities aligned to medical objectives and territory priorities.
- Use approved tools/channels/approaches to optimize exchange while maintaining full compliance.
- Ensure accurate, timely, compliant documentation per AbbVie policies and regulatory standards.
Qualifications:
- Advanced scientific degree required (PharmD, PhD, MD, PA, NP, or equivalent).
- Experience in Medical Affairs, clinical research, academic science, or other scientific/healthcare roles.
- Evidence-based scientific discussions with HCPs/scientific stakeholders (multiple myeloma preferred).
- Foundational disease/biologic/mechanism and standards of care knowledge.
- Working knowledge of clinical research principles, evidence types, and study design.
- Experience interpreting scientific literature/trial data/real-world evidence.
- Cross-functional collaboration experience.
- Travel up to 75%.
- Candidate must live in the territory or be willing to self-relocate within the territory.
Benefits (if eligible): paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k); eligible for long-term incentive programs.