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Regeneron

Associate Director, Field Medical Affairs – Hematology

Regeneron

Associate Director, Field Medical Affairs responsible for KOL engagement in hematology. Leading clinical information exchange and supporting clinical trials in Texas and surrounding areas.

Posted 6/21/2026full-timeRemote • Texas • 🇺🇸 United StatesSenior💰 $176,100 - $287,300 per yearWebsite

About the role

Key responsibilities & impact
  • 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

What you’ll need
  • 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.

Benefits

Comp & perks
  • annual bonuses or other incentive plans
  • equity awards
  • pension or retirement benefits
  • 401(k) company match
  • health and wellness programs
  • fitness centers
  • insurance benefits (e.g. medical, dental, vision, life and disability)
  • paid time off
  • family support benefits

ATS Keywords

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Hard Skills & Tools
clinical trials managementclinical research processesFDA regulationspharma regulationsOIG guidelinesdisease state knowledgetherapeutic area expertiseinvestigator-initiated study (IIS) supportscientific data presentationcompetitive intelligence reporting
Soft Skills
relationship buildingcommunicationcollaborationprofessionalismintegritystrategic thinkinginsight identificationproblem-solvingnetworkingadaptability
Certifications
MDPharmDPhDDNPDVM