Territory: Southern CA, TX, NV

Serving as a field-based extension of Company's, Medical Affairs. The Clinical Trial Liaison titled Clinical Research Medical Advisor (CRMA) will represent the Company and their investigational asset, currently in phase III clinical trial for myelofibrosis. The MSL will also handle pipeline products as their programs mature.

The CRMA will support the clinical trial program, in particular the Phase 3 trial through building credible peer to peer relationships through scientific/medical exchange with principal Investigators. Additionally, to build long term peer to peer relationships with, thought leaders, and other stakeholders specializing in Hematology/Oncology. The CRMA will support the Company’s advancing biopharmaceutical clinical and research programs by delivering clinical, scientific, and technical education to the Hematology/Oncology community. The CRMA is responsible for cultivating and maintaining collaborative relationships with leading members of the medical community to enhance company, disease state and clinical trial awareness, in addition to serving as an advanced technical, scientific, and medical expert in the Hematology/Oncology community for the assigned region. The CRMA is responsible for developing, coordinating, and assuring implementation of the Company’s corporate, scientific, and clinical strategies with these thought leaders within academic, clinical, and healthcare organizations. These scientific exchanges will support and/or expand current therapeutic concepts, as well as ensure the safe and effective utilization of the Company’s product(s).

The CRMA may support the Company’s research initiatives including Real World Data generation, and investigator-sponsored studies. They will also participate in and contribute to projects and initiatives that increase the value and productivity of the Medical Affairs team.

Duties and Responsibilities:

• Establish the Company as leaders committed to Hematology/Oncology, (and other therapeutic areas)
• Maintain clinical, scientific and technical expertise in relevant Hematology/Oncology (and other disease state areas)
• Provide enrolled sites with enrollment assistance, education and clinical support
• 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
• Identify and bring on new sites for consideration
• 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
• Identify barriers to clinical trial environment and recommend solutions to overcome these barriers
• Drive KOL/HCP development for launch readiness in accordance to the medical affairs plan
• Collaborate with medical affairs, clinical development, and commercial colleagues in a compliant manner, and serve as a resource to HCPs, large group medical practices
• Develop and track key opinion leader (KOL) engagement plans – identify, develop and maintain long-term collaborative relationships with KOLs within assigned region. Participate in medical and scientific exchanges with the medical/scientific community including advisory boards
• Provide medical/ clinical teams with feedback and insights from interactions with KOLs and investigators
• Respond to and document unsolicited requests for information on the Company products and clinical programs
• Support internal requests for dossier review and comment, medical review/consideration of potential business development opportunities and other unique projects as requested.
• Participate in/support the training of field and home office employees
• Facilitate research collaborations (including Real World Data [RWD] generation and investigator sponsored trials [IIS]) with key investigators including helping identify, establish, and maintain such collaborations
• Represent the company at medical meetings through Medical Affairs’ Scientific Booth coverage and other related activities
• Engage in speaker identification, training and evaluation and provide support for advisory board meetings as requested
• Adhere to corporate SOPs and ensure vigilant compliance with relevant legal and regulatory guidelines governing scientific interactions with physicians and healthcare professionals across all activities, including those related to clinical trials, scientific interactions with internal and external groups, and responses to unsolicited request for medical/ scientific information

Qualifications:

• An advanced degree required (Pharm D, PhD or MD) preferred
• A minimum of 2 years previous MSL experience strongly preferred
• A Minimum of 2 years of clinical or research experience in the area of Hematology or Oncology preferred
• Ability to travel, locally and regionally, up to 60% with overnight stays (e.g., KOL meetings, site locations, internal meetings, medical meetings and congresses, training)
• Experience working with payers of formulary committees strongly preferred
• Knowledge of local regulatory requirements and Pharmaceutical Association Code, including regulations governing compliant scientific exchange
• Demonstrated ability to integrate and work in cross functional network/matrix
• Demonstrated project management ability
• Excellent communication (oral and written) and interpersonal skills
• Valid driver’s license
• Must be able to proficiently communicate (oral and written) in English and other languages required by region