Sr. Medical Science Liaison
Johnson & JohnsonAbout the role
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Medical Affairs GroupJob Sub Function:
Medical Science LiaisonJob Category:
Scientific/TechnologyAll Job Posting Locations:
New York, New York, United StatesJob Description:
The Senior Medical Science Liaison (MSL) position is a field-based position covering the New York City, South region (North New Jersey, Lower Manhattan, Brooklyn, Queens) as the credible scientific expert representing ITCI in the healthcare community and will report directly to the Regional MSL Director, Northeast.
Job Responsibilities
Establishes strong relationships with key KOLs and practitioners in psychiatry
Understands region’s business needs and develops a robust field engagement plan to consistently meet or exceed team metrics
Takes on lead MSL responsibilities on team and individual projects, and serves as a coach/mentor to new team members
Works compliantly to provide high-level scientific support across company departments and in the field
Successfully completes scientific training curriculum including current therapeutic area and product knowledge relevant to ITCI
Master all MSL presentation content and with the ability to recognize and deliver on audience needs
As the subject matter expert, exhibits strong knowledge across the therapeutic area including research and clinical data, and contributes to MSL field content development
Engages in appropriate high-level, scientific exchange with the healthcare community including key stakeholders across managed markets and advocacy groups
Stays abreast of current literature, interprets, and effectively communicates complex concepts including key scientific and evidence-based data that address educational and research needs
Participates as the team lead across team projects and medical support responsibilities such as congress attendance, speaker support, insights report etc. as needed and delivers on individual responsibilities
Contributes to timely and relevant field insights, which enhance understanding of the scientific and clinical value of ITCI products
Able to think analytically and plan strategically with a results- and solutions-oriented mindset, contributing to team and medical affairs plans
Responds to unsolicited health care practitioner requests through appropriate use of approved materials
Collaborates effectively with timely and clear communications
Provides support to ITCI research initiatives and identifies business collaborations/interests regarding speaker, advisory or research/clinical expertise
Provides education and support to clinical site investigators involved in ITCI-sponsored trials, as needed
Executes on administrative tasks in a timely and compliant manner (e.g., expense reports, field activity reports, company vehicle documentation, compliance trainings and certifications)
Understands and contributes toward a positive team culture, promotes a cohesive work environment including participating in company’s/team’s work activities
Job Requirements
Advanced degree (Pharm.D., Ph.D., M.D.) and 3-6 years of MSL experience
Pharmaceutical industry experience preferred in CNS therapeutic area. Experience in schizophrenia, bipolar disorder, depression, and/or neurodegenerative disorders is preferred
Previous relevant experience in neuropsychiatric research/clinical practice and knowledge of pre-clinical/clinical aspects of drug development and approval processes preferred
Prior pro
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