Associate Director, Field Medical Affairs- Allergy (eastern states)
About the role
This is a pre-launch opportunity to join a newly formed field medical team. You will serve as the primary scientific presence in your territory, engaging in meaningful exchange of clinical data and medical information with key opinion leaders (KOLs), healthcare providers (HCPs), clinical research investigators, pharmacists, and other decision-makers. You will build investigator relationships, site infrastructure, and medical intelligence that shapes the program's clinical and medical trajectory. You will align field activities with strategic medical plans, gather actionable insights on the evolving treatment landscape, and support research and development that advances both the pipeline and patient outcomes.
Responsibilities
- Cultivate investigator relationships ahead of study activation to build scientific credibility and organizational trust.
- Maintain mapping of the KOL and investigator landscape in allergy/immunology to inform clinical and medical strategy.
- Collect and analyze early field insights into treatment patterns, unmet needs, and emerging science to shape the medical plan.
- Support the development of medical affairs infrastructure, including educational materials and scientific exchange tools, prior to launch.
- Act as a primary clinical/scientific resource to HCPs for disease-state and product information to ensure awareness and understanding.
- Establish, foster, and maintain peer relationships with KOLs in allergy/immunology.
- Identify and report medical insights.
- Identify research gaps and educational needs to inform medical strategy.
- Respond to requests for information related to study indications, disease states, and the therapeutic area, and discuss scientific and clinical data with appropriate audiences in a compliant manner.
- Ensure company policies, procedures, principles, and financial controls are upheld with integrity and professionalism.
Requirements
- A Clinical or scientific doctorate: MD, PharmD, PhD, DNP, or DVM is required.
- 8 years of experience in a relevant scientific, clinical, or pharmaceutical role, including 4+ years as a Medical Science Liaison in the pharmaceutical industry is required.
- Experience in allergy/immunology is required.
- Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharmaceutical compliance, and OIG guidelines.
- Ability to travel frequently (approximately 50%), including air travel, overnight stays, and occasional weekend travel.
- Prior experience in a pre-launch or launch phase MSL role is preferred.
- Experience supporting clinical trial site identification, feasibility assessment, or investigator engagement would be helpful.
Qualifications
To be considered for this role, you should thrive working independently, making a meaningful impact on the company's mission, and developing expertise in and sharing clinical and scientific data. You should enjoy building collaborative relationships across academic and clinical practice settings and balancing multiple initiatives, prioritizing amid ambiguity, and implementing independently while keeping partners engaged and informed. You should also be energized by pre-launch work and motivated by the opportunity to build investigator networks and scientific infrastructure from the ground up.
Skills
- Strong communication and interpersonal skills.
- Excellent scientific and clinical knowledge.
- Ability to manage multiple projects simultaneously.
- Strong analytical and problem-solving skills.
- Proficiency in Microsoft Office Suite.
Benefits
At Regeneron, we offer a competitive and comprehensive total rewards package which may include, depending on country and role:
- 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.
Pay
$176,100.00 - $287,300.00 annually
Schedule
On-site work is required.