Medical Science Liaison / Senior Medical Science Liaison - West / Midwest

Beeline Medicines

7d • $165,000 - $235,000 • Remote

About The Position

Beeline Medicines is a clinical-stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.

We are seeking talented field-based scientific professionals to join our Medical Affairs team as a Medical Science Liaison (MSL) or Senior Medical Science Liaison (Senior MSL) within our Immunology & Inflammation (I&I) therapeutic area. Both roles are central to building scientific awareness and advocacy for Beeline's pipeline, supporting investigator-initiated research, and facilitating meaningful peer-to-peer scientific exchange. The MSL level focuses on building foundational field excellence with progressive independence, while the Senior MSL operates with full strategic autonomy, leads senior KOL relationships, and contributes directly to Medical Affairs strategy and team development.

Requirements

• Advanced degree required — PharmD, PhD, or MD in a relevant life sciences, pharmacy, or biomedical field.
• Post-doctoral training, clinical fellowship, or residency in a relevant discipline strongly preferred.
• Minimum of 3 years of MSL or related field-based medical affairs experience in the pharmaceutical or biotech industry, with experience in immunology, inflammation, or a related therapeutic area strongly preferred.
• Clinical-stage biotech experience a plus.
• Developing scientific and clinical knowledge of immunology and inflammation — demonstrates foundational understanding of disease mechanisms, treatment landscapes, and emerging therapeutic approaches and is actively building depth through ongoing learning.
• Ability to interpret and communicate clinical and scientific data — including study design, statistical concepts, and benefit-risk assessment — in peer-to-peer HCP KME, and investigator settings, with continued development of sophistication over time.
• Working proficiency in CRM platforms (e.g., Veeva) for field activity documentation, HCP, KME, and investigator mapping, and territory management — developing consistent documentation habits that reflect compliance and organizational standards.
• Building knowledge of medical affairs compliance frameworks — including FDA and EMA regulations, PhRMA guidelines, and the distinctions between on-label and off-label scientific exchange — with active demonstration of compliant field behavior in all interactions.
• Developing field independence — operates with guidance from Medical Affairs leadership, demonstrates growing ability to manage territory priorities, plan engagement calendars, and execute field activities with increasing self-direction.
• Team contributor and active learner — engages constructively in MSL team discussions, shares field observations openly, and demonstrates intellectual curiosity and a growth mindset in building scientific and professional capabilities.
• Developing scientific communication skills — able to present and discuss Beeline's I&I data clearly and accurately with HCPs, KMEs and investigators, with active development of the depth, nuance, and adaptability that characterizes expert-level scientific dialogue.
• Building active listening and field intelligence skills — demonstrates growing ability to capture insights and clinical practice observations accurately and translate them into concise, useful internal communications.
• Growing confidence in varied engagement settings — developing effectiveness in one-on-one HCP/KME/investigator meetings, small group scientific discussions, and conference interactions, with continued development toward advisory board and large group facilitation.
• Ability to safely and successfully operate a motor vehicle is required. Valid US Driver’s License and a driving record in compliance with company standards
• Minimum of 5 years of MSL or field-based medical affairs experience in the pharmaceutical or biotech industry, with demonstrated expertise in immunology, inflammation, or a closely related therapeutic area preferred.
• Prior involvement in IIS management or clinical trial support activities preferred.
• Advanced scientific and clinical expertise in immunology and inflammation — demonstrates deep, current knowledge of disease biology, treatment algorithms, clinical trial endpoints, emerging mechanisms, and the competitive I&I landscape, applied with confidence in complex scientific discussions.
• Expert ability to interpret, contextualize, and communicate complex clinical and translational data — including study design nuances, subgroup analyses, and evolving safety/efficacy profiles — in substantive peer-level discussions with senior KOLs and investigators.
• Established proficiency in Veeva CRM and medical affairs field tools; experience with digital engagement platforms and virtual scientific exchange, with consistent documentation quality that reflects field excellence standards.
• Leverage AI-driven and omnichannel engagement strategies to complement in-person interactions; optimizing reach, frequency, and scientific exchange effectiveness with key stakeholders.
• Deep working knowledge of medical affairs compliance — including PhRMA guidelines, FDA regulations, and IIS management frameworks — demonstrated through a sustained record of compliant, high-quality field interactions and the ability to guide junior colleagues on compliance questions.
• Operates with full strategic independence — manages territory, KOL engagement plans, and field priorities without day-to-day guidance; proactively identifies opportunities and addresses challenges with sound judgment and organizational awareness.
• Highly sophisticated scientific communicator — engages senior KOLs, principal investigators, and academic thought leaders in nuanced, data-rich scientific dialogue that builds long-term credibility and trust for Beeline's I&I platform.
• Skilled at synthesizing and presenting complex field intelligence in structured, executive-ready internal communications — delivers strategic actionable recommendations and tracking downstream impact to refine engagement strategy and maximize organizational value to Medical Affairs and clinical leadership with clarity and confidence.
• Experienced facilitator and presenter — equally effective in one-on-one KOL settings, investigator meetings, advisory board participation, and large medical congress environments, with a demonstrated ability to adapt scientific communication style to audience needs.

Nice To Haves

• Clinical-stage biotech experience a plus.
• Clinical-stage biotech experience a plus

Responsibilities

• Contribute to development and refinement of medical strategy through field insights and HCP, KME, and investigator engagement.
• Develop and execute territory plans aligned with organizational priorities and data milestones.
• Develop and manage a defined territory of KME and HCP relationships within the I&I therapeutic area — identifying, mapping, and engaging scientific thought leaders, clinical investigators, and academic centers relevant to Beeline's pipeline under the direction of Medical Affairs leadership.
• Lead segmentation (Tier 1/2/3) development, strategic engagement plans and longitudinal relationship ownership with HCPs, KMEs, and investigators.
• Conduct peer-to-peer scientific exchange with KMEs, HCPs, and clinical investigators — sharing clinical and preclinical data, presenting pipeline updates, and discussing unmet medical needs in I&I in a balanced, compliant, and scientifically rigorous manner.
• Support clinical trial awareness and site identification efforts by engaging with potential investigators and academic institutions, facilitating scientific discussions that may support site initiation and patient enrollment for organization’s I&I programs. Serve as the key resource for scientific exchange as the ‘face of the sponsor’ with clinical site investigators from site start-up through end of study closeout in close collaboration with Clinical Operations.
• Respond to unsolicited medical information requests from HCPs, KMEs, and/or investigators in a timely, accurate, and compliant manner — in partnership with Medical Information and in accordance with applicable regulatory and compliance guidelines.
• Serve as the field-based scientific resource for HCP, KME and investigator interactions related to investigator-initiated studies (IIS) — supporting the IIS process by facilitating scientific discussions and coordinating with internal Medical Affairs leadership.
• Support identification of evidence gaps and contribute to evidence generation strategies.
• Generate, synthesize, and translate insights into strategic recommendations, with a focus on quality and actionability — including KME perspectives, competitive intelligence, clinical practice trends, and unmet need observations — back to Medical Affairs, Clinical Development, and other cross functional teams in a structured and timely manner.
• Represent Beeline at scientific conferences, medical congresses, and advisory board meetings within the I&I therapeutic area — engaging with scientific thought leaders and gathering data that informs the organization's medical and pipeline strategy.
• Perform other duties and responsibilities as assigned.
• Lead and manage a strategically defined territory of senior KOL, clinical investigator, and academic center relationships — developing long-term, individualized engagement plans that align KOL scientific interests with organizations pipeline priorities and medical affairs objectives with full independence. Develop and continuously refine territory strategy based on evolving data milestones, KME influence mapping, and clinical development priorities; ensuring optimal allocation of time and resources to maximize impact.
• Conduct sophisticated, peer-to-peer scientific exchange with senior thought leaders, clinical investigators, and HCPs — including discussions of emerging clinical data, nuanced benefit-risk considerations, and evolving disease paradigms relevant to organization's I&I programs.
• Serve as a senior field resource for clinical trial support — including investigator identification, scientific site engagement, and contributions to enrollment strategy discussions in close collaboration with Clinical Development and Clinical Operations.
• Own and manage investigator-initiated study (IIS) relationships within the territory — serving as the primary scientific point of contact for investigators, facilitating the IIS review process, and maintaining ongoing scientific engagement with funded IIS sites.
• Proactively synthesize and present strategic KOL engagement insights and field intelligence — delivering actionable recommendations to Medical Affairs leadership, Clinical Development, and other strategy teams that influence organizational decision-making. Demonstrate measurable impact on key Medical Affairs priorities, including KME engagement quality, contribution to clinical trial enrollment and site activation, and influence on strategic decision-making through actionable field insights.
• Contribute to the development of MSL scientific training materials, field tools, and disease area resources — applying territorial expertise and scientific depth to strengthen the broader MSL team's capabilities and field effectiveness.
• Represent Beeline at major national and international scientific conferences, advisory boards, and KOL forums within I&I — serving as a senior scientific ambassador with the credibility and confidence to engage the field's most influential voices. Play a leadership role in advisory board development and execution; including KME identification, scientific input into agenda design, and synthesis of outcomes into strategic recommendations.

Benefits

• Medical, Dental & Vision insurance (employee premiums 100% covered by company)
• 20 accrued days combined time off (PTO/Sick), 12 company holidays, & winter recharge
• Flexible work arrangements / hybrid schedule
• Health Savings Account (HSA)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level