Medical Science Liaison, Hematology/Rare Disease (Central)

Job #: 3720Company: TMACPosted: Friday, September 18, 2026Serving as a value, added, field-based resource, and extension of Company's Medical Affairs team, the Clinical Trial Liaison (CTL) will play a crucial role in the execution of clinical trials. In this pivotal position, the CTL will provide essential support to Company's Global Clinical Sciences and Operations teams, contributing significantly to the success of their clinical research initiatives, specifically to the success of the phase III program, evaluating the safety and efficacy of company's asset.Duties and Responsibilities:Drive awareness and enrollment of patients, ensuring that they provide the investigators and site staff with relevant, compliant, and consistent medical and scientific support and communications Provide in-depth drug and disease state medical and scientific information to HCPs. Conduct targeted conversations with the investigators and site staff regarding operational challenges, including but not limited to those related to patient recruitment and retention. Actively participate in supporting and driving recruitment and enrollment with sites in collaboration with Clinical Operations and CRO teams.Maintain clinical, scientific, and technical expertise in relevant rare hematology disorders with a focus on chronic neutropenia.Engage with investigators and other site personnel at sites to ensure they are familiar with all protocol and patient information as well as serve as a local clinical expert and support clinical operations efforts.Identify and recommend new sites for consideration for trial participation. Support feasibility, site selection and present scientific and medical disease background, protocol and other study/disease relevant material at the site initiation visits (SIVs)Identify barriers to clinical trial environment and recommend solutions to overcome these barriers and contribute to study recruitment strategyProvide medical/clinical teams with feedback and insights from interactions with KOLs and investigators pertaining to trial and other scientific narrativesAdditionally, the CTL may also participate in and contribute to projects and initiatives that increase the value and productivity of the Medical Affairs teamRepresent the company at medical meetings through Medical Affairs’ Scientific Booth and sessions/posters/CI coverage and other related activitiesOther duties/responsibilities as assignedQualifications:Advanced degree (PharmD, PhD, MD, NP, PA) or equivalent terminal degree with appropriate clinical experience and scientific background requiredPrior experience as an MSL/CTL (3-5 years); preferably with a clinical trial focus in a pre-launch setting requiredPrior Rare disease and/or immunology and/or hematology experience preferredProven ability to engage Investigators/KOLs in non-promotional, scientific exchangePrior clinical operations, site level trial execution, and CRO experience preferredAbility to travel, locally and regionally, up to 50% with overnight stays (car, plane, train) Knowledge of local regulatory requirements and Pharmaceutical Association Codes, including regulations governing compliant scientific exchangeDemonstrated ability to integrate and work in cross functional network/matrixDemonstrated project management abilityExcellent communication (oral and written) and interpersonal skillsMust be able to proficiently communicate (oral and written) in English and other languages required by region Valid driver’s license