MSL/Sr. MSL Oncology, Multiple Myeloma (California)
AbbVie
June 30, 2026
On-site
Los Angeles, CA
$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 of AbbVie’s therapeutic areas through high-quality, non-promotional scientific exchange.
Responsibilities:
- Deliver high-quality, balanced, and compliant scientific exchange tailored to clinical context and informational needs.
- Build and sustain credible scientific relationships for meaningful two-way dialogue and Scientific Intelligence.
- Interpret and communicate 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 awareness of clinical research and engaging investigators where appropriate.
- Translate complex scientific/clinical information into clear discussions aligned to stakeholder needs.
- Collaborate with Medical Affairs, Health Impact (MHI), Clinical Development, Evidence Generation partners, and the In-Field team (IFT).
- Plan and execute scientific engagement aligned to medical objectives and territory priorities.
- Use approved tools/channels to optimize scientific exchange while maintaining compliance.
- Ensure accurate, timely, compliant documentation of scientific interactions and Scientific Intelligence.
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 stakeholder engagement experience (multiple myeloma preferred).
- Foundational disease/mechanism-of-action/standards-of-care knowledge.
- Working knowledge of clinical research principles, evidence types, and study design.
- Ability to interpret scientific literature, clinical trial data, or RWE.
- Cross-functional collaboration experience.
- Travel up to 75%.
Competencies/Skills:
- Communicates scientific data accurately and clearly.
- Interprets evidence to support discussions and stakeholder questions.
- Uses structured planning to align engagement with objectives/territory priorities.
- Delivers compliant, two-way scientific exchange.
Note: Candidate must live in the territory or be willing to self-relocate within the territory.
Benefits:
- Paid time off; medical/dental/vision insurance; 401(k) (eligible employees).
Responsibilities:
- Deliver high-quality, balanced, and compliant scientific exchange tailored to clinical context and informational needs.
- Build and sustain credible scientific relationships for meaningful two-way dialogue and Scientific Intelligence.
- Interpret and communicate 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 awareness of clinical research and engaging investigators where appropriate.
- Translate complex scientific/clinical information into clear discussions aligned to stakeholder needs.
- Collaborate with Medical Affairs, Health Impact (MHI), Clinical Development, Evidence Generation partners, and the In-Field team (IFT).
- Plan and execute scientific engagement aligned to medical objectives and territory priorities.
- Use approved tools/channels to optimize scientific exchange while maintaining compliance.
- Ensure accurate, timely, compliant documentation of scientific interactions and Scientific Intelligence.
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 stakeholder engagement experience (multiple myeloma preferred).
- Foundational disease/mechanism-of-action/standards-of-care knowledge.
- Working knowledge of clinical research principles, evidence types, and study design.
- Ability to interpret scientific literature, clinical trial data, or RWE.
- Cross-functional collaboration experience.
- Travel up to 75%.
Competencies/Skills:
- Communicates scientific data accurately and clearly.
- Interprets evidence to support discussions and stakeholder questions.
- Uses structured planning to align engagement with objectives/territory priorities.
- Delivers compliant, two-way scientific exchange.
Note: Candidate must live in the territory or be willing to self-relocate within the territory.
Benefits:
- Paid time off; medical/dental/vision insurance; 401(k) (eligible employees).