Responsibilities:

• Identify, develop, and maintain strong, scientific, peer-to-peer relationships with academic and community research thought leaders, appropriate HCPs, and access stakeholders, within a given geography to answer scientific and product related questions
• Act as the primary point of contact for scientific exchange between Orca Bio and the medical community, answering scientific and product-related questions
• Engage in meaningful scientific exchange that will ensure patients have access to Orca Bio medicines, to ensure their safe and appropriate use through peer-to-peer discussions aligned with medical strategies and needs expressed by external stakeholders, and to facilitate research
• Actively assess the medical landscape by meeting with TL/HCPs to understand their needs and expertise
• Collaborate with cross-functional teams including Clinical Development, Regulatory Affairs, and Commercial to support product development and commercialization efforts
• Provide scientific and clinical expertise to support internal and external stakeholders, demonstrating an understanding of the Clinical and Regulatory requirements specific to a field-based medical organization
• Ensure compliance with regulatory and company policies in all interactions and communications, while also utilizing expertise in developing clinical presentations and medical education materials to effectively disseminate scientific information
• Support clinical trial activities to enhance patient recruitment, enrollment and/or discussions around the safe and effective use of Orca Bio investigational products, leveraging clinical trial experience and knowledge of Good Clinical Practice (GCP) to ensure adherence to ethical and regulatory standards
• Provide recommendations and insights to clinical development team on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators
• Act as the primary liaison to investigators interested in developing, submitting and performing Investigator-Sponsored Trials (IST)
• Attend and provide scientific support at medical congresses and at regional, national, and international meetings
• Collect and provide meaningful medical insights and/or impact by communicating these back to the medical organization to support strategy development
• Provide medical and scientific support of the strategy of health outcomes, real-world evidence, and payer/provider engagements
• Work in conjunction with the appropriate internal teams to support Orca Bio’s collaboration and interactions with professional organizations/societies & advocacy groups, GPOs, and large networked practices
• Support advisory boards, clinical investigator meetings, and educational forums, organizing and chairing roundtable and educational meetings as needed
• Collaborate with internal colleagues and KOLs/HCPs on Medical Affairs initiatives including publications as requested, advisory boards, medical meeting support, medical education opportunities, training, etc.
• Provide education and training to commercial marketing and sales teams on therapies and disease states
• Respond to medical inquiries

Requirements:

• Advanced degree (PhD, PharmD, MD, DNP or equivalent) in a relevant scientific discipline
• 5+ years of relevant clinical experience (malignant hematology, bone marrow transplant, or cellular therapy) required
• 5+ years of experience in the pharmaceutical or biotechnology industry as a Medical Science Liaison preferred
• Strong understanding of clinical development, regulatory requirements, and commercial strategies
• Excellent interpersonal and communication skills, with the ability to engage and influence a wide range of stakeholders
• Demonstrated ability to interpret and present complex scientific data to diverse audiences
• Strong strategic thinking and problem-solving skills
• Demonstrated ability to expertly collaborate with cross-functional colleagues in order to best serve the needs of external stakeholders
• Ability to work independently and manage multiple priorities in a fast-paced, dynamic environment
• Clinical trial experience with working knowledge of Good Clinical Practice (GCP)
• Understanding of the Clinical and Regulatory requirements in a field-based medical organization
• Experienced in key opinion leader development to establish and maintain peer-to-peer relationships-with established relationships in given territory
• Expertise in developing clinical presentations and medical education