Medical Science Liaison Director

6 days ago

Durham, North Carolina, United States Eisai Inc. Full time
Job Summary

Eisai Inc. is seeking a highly motivated and experienced Medical Science Liaison Director to lead our East Region team in the GI/GU and Oncology areas. As a key member of our Medical Affairs team, you will be responsible for ensuring operational excellence, providing leadership, and developing individual talent within the MSL region.

Key Responsibilities
  • Ensure operational excellence of the MSL team, including corporate aligned objective/tactics, cross-functional medical support, and interactions with key opinion leaders.
  • Provide leadership for the MSL function by participating on cross-functional teams leading to strategic planning and working collaboratively with Commercial colleagues including, Sales and Marketing as well as Medical Affairs.
  • Developing individual talent within the MSL region, including training, career evaluation, coaching, mentoring, performance management and talent review.
  • Ensure compliance with regulatory and other ethical guidelines relevant to the pharmaceutical industry, and to ensure compliance with Eisai policies & procedures and standard operating procedures.
  • Manage MSL activities related to presenting medical and scientific information to external customers, including but not limited to, medical thought leaders, academic institutions and managed care organizations.
  • Assist with recruiting, interviewing hiring, and on-boarding new MSLs.
  • Travel (up to approx. 50%), locally across the US when required and including international travel.
Requirements
  • Advanced scientific terminal degree (MD, PhD, PharmD)
  • Must have a minimum of 5 years of experience within the pharmaceutical industry overseeing a Medical Science Liaison team or related function.
  • Excellent interpersonal, communication, and management skills required.
  • Strong personal integrity and customer focus are necessary.
  • Ability to work at a distance to maintain morale of field based personnel, as well as good interaction with office based Medical Affairs and PCU scientific staff.
  • Must possess a thorough understanding of the FDA, OIG, HIPPA, PhRMA, GCP and other international regulatory/ethical guidelines relevant to the pharmaceutical industry & clinical trial conduct, and to ensure compliance with these external as well as internal Eisai guidelines and standard operating procedures.
  • Must be able to organize, prioritize, and work effectively in a constantly changing environment
  • Ability to interface effectively with a variety of technical platforms for recording of external interactions and for the collection, review, and dissemination of medical information.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status.

Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States.

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