The Medical Affairs Company (TMAC)
Medical Science Liaison, Hematology / Oncology (West region)
The Medical Affairs Company (TMAC), San Francisco, California, United States, 94199
Serving as a value-added, field-based resource and extension of the Company's Medical Affairs, the Medical Science Liaison (MSL) plays a crucial role in executing clinical trials. In this position, the MSL provides essential support to teams contributing significantly to research success. The company's pioneering drug is in Phase I/II clinical trials for hematological malignancies, addressing major clinical unmet needs and offering new therapy options for cancer patients.
Read on to fully understand what this job requires in terms of skills and experience If you are a good match, make an application. Essential Duties and Responsibilities : Establish the company as a clinical-stage biotech organization that is science-driven and patient-focused, leading in the inhibition of p300 / CBP to treat specific cancers, notably multiple myeloma. Maintain clinical, scientific, and technical expertise in relevant oncology therapies and treatment areas. Collaborate with Medical Affairs, Clinical Operations, and other internal stakeholders, serving as a resource to external stakeholders. Work with clinical sites to enhance patient identification and enrollment activities for the company's clinical trials. Engage with investigators and site staff to ensure clinical trials are prominent, differentiated, and that staff are familiar with protocols and patient information. Provide investigators and site staff with compliant, relevant, and consistent medical and scientific support and communication. Develop and monitor KOL engagement plans; identify, develop, and maintain relationships with KOLs within the assigned region. Participate in scientific exchanges with the medical community. Gather and relay feedback and insights from interactions with KOLs and investigators to the medical/clinical teams. Respond to unsolicited information requests regarding the company's clinical programs and document these interactions. Support Medical Affairs in special projects related to medical communications, publication materials, and training initiatives. Represent the company at medical conferences through thought leader meetings, symposia, and competitive intelligence activities. Qualifications : Advanced terminal degree (PharmD, PhD, DNP, or MD) preferred; NP, MSN, or PA with Hematology/Oncology and MSL experience will be considered. At least 3+ years of Oncology MSL experience, preferably in Multiple Myeloma. Minimum of 5+ years of clinical and/or research experience in Oncology. Established relationships with Oncology KOLs and stakeholders at academic and community practices preferred. Ability to travel up to 60% locally and regionally, including overnight stays. Experience working with payers and formulary committees is preferred. Knowledge of FDA regulations, PhRMA Code, and compliant scientific exchange requirements. Ability to work effectively in cross-functional teams and manage projects. Valid driver's license required. COVID-19 Vaccination Requirements : This role requires visiting customer sites, which may have COVID-19 vaccination policies. Proof of vaccination may be required. Salary will be determined based on experience, education, and therapeutic expertise.
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Read on to fully understand what this job requires in terms of skills and experience If you are a good match, make an application. Essential Duties and Responsibilities : Establish the company as a clinical-stage biotech organization that is science-driven and patient-focused, leading in the inhibition of p300 / CBP to treat specific cancers, notably multiple myeloma. Maintain clinical, scientific, and technical expertise in relevant oncology therapies and treatment areas. Collaborate with Medical Affairs, Clinical Operations, and other internal stakeholders, serving as a resource to external stakeholders. Work with clinical sites to enhance patient identification and enrollment activities for the company's clinical trials. Engage with investigators and site staff to ensure clinical trials are prominent, differentiated, and that staff are familiar with protocols and patient information. Provide investigators and site staff with compliant, relevant, and consistent medical and scientific support and communication. Develop and monitor KOL engagement plans; identify, develop, and maintain relationships with KOLs within the assigned region. Participate in scientific exchanges with the medical community. Gather and relay feedback and insights from interactions with KOLs and investigators to the medical/clinical teams. Respond to unsolicited information requests regarding the company's clinical programs and document these interactions. Support Medical Affairs in special projects related to medical communications, publication materials, and training initiatives. Represent the company at medical conferences through thought leader meetings, symposia, and competitive intelligence activities. Qualifications : Advanced terminal degree (PharmD, PhD, DNP, or MD) preferred; NP, MSN, or PA with Hematology/Oncology and MSL experience will be considered. At least 3+ years of Oncology MSL experience, preferably in Multiple Myeloma. Minimum of 5+ years of clinical and/or research experience in Oncology. Established relationships with Oncology KOLs and stakeholders at academic and community practices preferred. Ability to travel up to 60% locally and regionally, including overnight stays. Experience working with payers and formulary committees is preferred. Knowledge of FDA regulations, PhRMA Code, and compliant scientific exchange requirements. Ability to work effectively in cross-functional teams and manage projects. Valid driver's license required. COVID-19 Vaccination Requirements : This role requires visiting customer sites, which may have COVID-19 vaccination policies. Proof of vaccination may be required. Salary will be determined based on experience, education, and therapeutic expertise.
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