Senior Medical Science Liaison, Eastern Corridor (PA, NJ, VA, DE, MD, DC)

Role Summary

The Sr. MSL is a key member of Global Medical Affairs, communicating scientific, clinical and technical information within the medical community, developing and maintaining strong collaborative relationships with Key Opinion Leaders and serving as a therapeutic and radiopharmaceutical expert with internal audiences. Preferred candidates will reside near an international airport. This is a remote position open to applicants authorized to work for any employer within the United States.

Responsibilities

• Identifies, develops and maintains long term collaborative relationships with Key Opinion Leaders in assigned territory.
• Demonstrates strong communication skills with the ability to present approved scientific data of varying levels of complexity to internal and external customers in both group and one-to-one settings, appropriately adjusted to the audience and in accordance with Company Policies, and applicable laws, regulations and ethical standards.
• Demonstrates appropriate response and documents the provision of accurate, approved scientific data in response to unsolicited scientific questions or requests posed by internal and external customers for approved Products/Brands and for products in development in accordance with Company Policies, and applicable laws, regulations and ethical standards.
• Shares appropriate approved clinical/technical information in a timely manner with the appropriate functional teams and other internal personnel.
• Utilizes advanced clinical and technical expertise in contacts with External Experts, in accordance with the strategy developed by the Company and Compliance Policies to further understand and gain insight into (1) diagnostic medical imaging patterns in prostate cancer (2) treatment guidelines and therapeutic advances in the oncology arena, (3) the needs and interests of Healthcare providers, and (4) the medical needs of patients.
• Identifies potential speakers for promotional programs and speaker training meetings.
• Provides constructive feedback to speakers and Lantheus (e.g., Professional Promotions) regarding accuracy and delivery of approved presentations and adherence to Compliance Policies.
• Fully understands and complies with Lantheus Pharmacovigilance SOPs regarding Adverse Events.
• Identifies potential investigators for investigator sponsored trials following approved processes.
• Adheres to the US ‚ÄúCompliance Code of Conduct‚Äù and all LMI policies and procedures, the OIG Guidance, the PhRMA Code, GCP, HIPAA and relevant FDA laws and regulations (certify completion where required).

Qualifications

• PhD, PharmD or MD required.
• 4+ years MSL experience preferred.
• 2 + years Clinical experience in oncology, urology or radiopharmaceuticals/medical imaging preferred.
• Advanced understanding of current and emerging trends in the field of oncology, radiopharmaceuticals and diagnostic imaging.
• Proficient at translating approved scientific or clinical data into high quality medical information to help Healthcare providers best serve their patients.
• Demonstrated leadership working in a team environment with the ability to communicate effectively with management, peers, and all cross-functional teams.
• Highly motivated to achieve optimal results with a demonstrated record of growth and achievement.
• Proven ability to successfully manage multiple tasks simultaneously and adapt to and communicate change.
• Exceptional communicator and presenter with proven oral and written communications skills.

Other Requirements

• Oncology and/or Radiopharmaceutical knowledge, including key scientific publications
• In-depth knowledge of a technical, scientific or clinical area
• Knowledge of clinical trial design and process
• Knowledge of principles and implications of pharmacoeconomic data
• Advanced knowledge of the US Healthcare System and the Medical Imaging industry
• Advanced Word, PowerPoint, and Excel skills
• 70% Travel required; reside near a major airport