Associate Director, Medical Affairs- Allergy & Immunology

Location
Tarrytown, New York
Posted
Apr 11, 2018
Ref
12520BR
Required Education
Doctorate/PHD/MD
Position Type
Full time
Position Summary

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases.

Summary
Provides scientific exchange and collaborations with leaders on disease and product information as well as research initiatives. Participates in the development and the management of company and investigator sponsored clinical trials. In support of scientific commercialization initiatives, presents scientific and clinical data in response to requests for information related to study indications and disease state awareness to opinion leaders, practitioners, investigators, research coordinators, site personnel and internal study stakeholders.
  • Participates in the development of company and investigator sponsored clinical trials including:
    • Concept proposals / Protocol development and review/ Site selection/ Investigator identification.
      • Act as a scientific resource for area healthcare professionals within the surrounding trial site community
      • Consults with physicians, pharmacists and other medical professionals to refer appropriate patients to Clinical Trial sites and review clinical practice topics as requested by the customer.
  • Scientific exchange and collaboration with therapeutic area experts on research initiative as well as disease and product information.
  • Present relevant scientific and clinical data to appropriate audiences which are consistent with compliance guidelines
  • Disease management consultation and education for the therapeutic area with identified practitioners, payers and researchers
  • Identifies gaps in research needs of company and create opportunities for the organization to fill those gaps by collaborating with potential and existing investigators.
  • Assists with management of clinical data through support of abstracts, posters, presentations and manuscript development to ensure rapid and accurate communication of scientific and clinical results.
  • Presents scientific and clinical data in response to requests for information related to study indications and disease state awareness to investigators, research coordinators, site personnel and internal study stakeholders.
  • Performs disease management consultations and provides education for the therapeutic area with identified researchers.
  • Ensures company policies, principles and financial controls are maintained with integrity and professionalism being displayed internally and externally.
  • Appropriately engages healthcare professionals and attends medical conferences to collect and report relevant competitive intelligence.
  • Collaborates with Clinical and other study staff to execute plans and strategies established by Medical Affairs.
  • Appropriately engages healthcare professionals and attends medical conferences to collect and report relevant competitive intelligence.
  • Support Commercialization Initiatives of approved products in covered therapeutic areas.
    • Train Commercial colleagues when appropriate
    • Provide scientific input upon request.


Education:
  • MD, PhD or PharmD from an accredited US or foreign medical school with three or more years of postgraduate medical training.
  • If an MD, preferably board certified in internal medicine, ideally with fellowship training in allergy, immunology, pulmonology, or related discipline desirable. If not an MD, experience in allergy, asthma, or dermatology.
  • Ability to travel extensively.
Experience:
  • At least ten (10) years total experience post medical degree, including clinical practice, with at least five to seven years progressive experience in Pharmaceutical or Biotech Industry working in Medical Affairs and/or Clinical Research & Development or related fields.
  • Industry experience in planning, executing and reporting clinical trials desirable with post-marketing experience a plus.
  • Prior experience working in a matrix organization as well as cross-functional collaboration with commercial/marketing departments strongly desired.
  • Experience working with field-based colleagues/MSLs.
  • US and global experience preferable.
  • Experience working corroboratively and coordinating with external partners.
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This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.

To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Requisition Number: 12520BR