Associate Director, Field Medical Affairs-Hematology ( TN, AL, MS, AR)

As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. We are expected to demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. 

Territory:  Tennessee, Alabama, Mississippi and Arkansas (residency in the territory is required with a preference of TN and AL.  

A typical day may include the following: 
•    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

This may be for you if you:
•    Want to be a part of a pre-launch stage team potentially for multiple launches.
•    Are skilled in the art of strategic conversation along with a proven ability to assess issues adapting appropriately.
•    Can demonstrate an understanding of “know your audience” and ability to tailor information appropriately.
•    Have demonstrated the ability to anticipate, organize, plan and handle multiple priorities, while adapting to the needs of the company.

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. 

Additional requirements: 
•    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.

Preferred experiences include: 
•    Established relationships with KOLs and institutions focused on Hematologic Malignancies
•    Drug launch experience. 
 

 

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

 

Where necessary, we disclose salary ranges for roles in all countries in which we operate.  The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.  Regeneron offers 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, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process.  If you have any questions, please speak with your recruiter. 

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$176,100.00 - $287,300.00