The Medical Affairs Company (TMAC)
Medical Science Liaison, Hematology (West region)
The Medical Affairs Company (TMAC), Phoenix, Arizona, United States, 85003
Medical Science Liaison, Hematology (West region)
This range is provided by The Medical Affairs Company (TMAC). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$170,000.00/yr - $190,000.00/yr Responsibilities
Establish Company as a clinical stage biotech company; science driven; patient focused. They lead 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 Company’s Medical Affairs, Clinical Operations, and other relevant internal stakeholders, and serve as a resource to external stakeholders. Collaborate with the clinical sites to enhance activities related to patient identification and enrollment into Company’s clinical trial. Engage with investigators and site staff to ensure clinical trial is maintained at a prominent level and is differentiated from competing protocols; and that they are familiar with all protocol and patient information. Provide the investigators and site staff with relevant, compliant, and consistent medical and scientific support and communications. Develop and track KOL engagement plans – identify, develop, and maintain collaborative relationships with KOLs within assigned region. Participate in medical and scientific exchanges with the medical/scientific community. Provide medical/clinical teams with feedback and insights from interactions with KOLs and investigators. Respond to and document unsolicited requests for information on Company’s clinical program. Support Medical Affairs by participating in special projects related to medical communications, publication materials, training initiatives, as requested. Represent the company at medical conferences through thought leader meetings, symposia attendance, competitive intelligence gathering and other related activities. Qualifications
Advanced terminal degree is strongly preferred (PharmD, PhD, DNP or MD). Will consider NP, MSN, or PA with Hematology/Oncology and MSL experience. Minimum of 3+ years previous Hematology/Oncology MSL experience required (Multiple Myeloma, preferred) Minimum of 5+ years of clinical and/or research experience in Oncology required. Established relationships with Oncology KOLs and stakeholders at both academic institutions and community practices preferred. Ability to travel, locally and regionally, up to 60% with overnight stays (e.g., KOL meetings, site locations, internal meetings/trainings, medical congresses) required. Experience collaborating with payers of formulary committees preferred. Knowledge of FDA requirements and PhRMA Code, including regulations governing compliant scientific exchange required. Demonstrated ability to integrate and work in cross functional network/matrix required. Demonstrated project management ability required. Valid driver’s license An essential function of this role is being able to support and visit customer’s sites and locations (hospitals, institutions). If such customers or locations have a COVID-19 policy that requires vaccination against COVID-19 or accepts exemptions, you may be asked to provide proof. Salary offers to be determined based on industry experience, education and therapeutic expertise. Seniority level
Associate Employment type
Full-time Job function
Research and Science Industries
Research Services
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This range is provided by The Medical Affairs Company (TMAC). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$170,000.00/yr - $190,000.00/yr Responsibilities
Establish Company as a clinical stage biotech company; science driven; patient focused. They lead 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 Company’s Medical Affairs, Clinical Operations, and other relevant internal stakeholders, and serve as a resource to external stakeholders. Collaborate with the clinical sites to enhance activities related to patient identification and enrollment into Company’s clinical trial. Engage with investigators and site staff to ensure clinical trial is maintained at a prominent level and is differentiated from competing protocols; and that they are familiar with all protocol and patient information. Provide the investigators and site staff with relevant, compliant, and consistent medical and scientific support and communications. Develop and track KOL engagement plans – identify, develop, and maintain collaborative relationships with KOLs within assigned region. Participate in medical and scientific exchanges with the medical/scientific community. Provide medical/clinical teams with feedback and insights from interactions with KOLs and investigators. Respond to and document unsolicited requests for information on Company’s clinical program. Support Medical Affairs by participating in special projects related to medical communications, publication materials, training initiatives, as requested. Represent the company at medical conferences through thought leader meetings, symposia attendance, competitive intelligence gathering and other related activities. Qualifications
Advanced terminal degree is strongly preferred (PharmD, PhD, DNP or MD). Will consider NP, MSN, or PA with Hematology/Oncology and MSL experience. Minimum of 3+ years previous Hematology/Oncology MSL experience required (Multiple Myeloma, preferred) Minimum of 5+ years of clinical and/or research experience in Oncology required. Established relationships with Oncology KOLs and stakeholders at both academic institutions and community practices preferred. Ability to travel, locally and regionally, up to 60% with overnight stays (e.g., KOL meetings, site locations, internal meetings/trainings, medical congresses) required. Experience collaborating with payers of formulary committees preferred. Knowledge of FDA requirements and PhRMA Code, including regulations governing compliant scientific exchange required. Demonstrated ability to integrate and work in cross functional network/matrix required. Demonstrated project management ability required. Valid driver’s license An essential function of this role is being able to support and visit customer’s sites and locations (hospitals, institutions). If such customers or locations have a COVID-19 policy that requires vaccination against COVID-19 or accepts exemptions, you may be asked to provide proof. Salary offers to be determined based on industry experience, education and therapeutic expertise. Seniority level
Associate Employment type
Full-time Job function
Research and Science Industries
Research Services
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