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Key Responsibilities
• Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action.
• Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies.
• Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding.
• Participates in the development and management of company sponsored clinical trials including.
• Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program.
• Identifying relevant insights on research developments, treatment landscape to shape medical strategy.
• Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel.
• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data.
• Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence.
• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally.
Requirements
• To be considered a terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.
• 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required.
• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines.
• Residency in the assigned territory.
• Travel: Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.
• Possesses and maintains a valid driver’s license and clean driving record.