(Sr.) Medical Science Liaison, Solid Tumor - Southern CA

MENARINI Group•Bridgewater, NJ

2d•$208,000 - $245,000•Remote

About The Position

Menarini Stemline is hiring a (Sr.) Medical Science Liaison for Southern California and Hawaii. The MSL conducts scientific exchange about Stemline’s pipeline, disease-state awareness, and scientific data with key opinion leaders (KOLs) and healthcare providers (HCPs). The role supports research interests involving company-sponsored trials and investigator-initiated research, provides fair and balanced medical information and clinical/scientific support, and supports safety education for HCPs and allied health professionals regarding Stemline products in approved indications. The position represents Stemline in its assigned territory, develops relationships with academic and community healthcare providers, and works with internal medical, clinical operations, commercial, and other stakeholders. It includes supporting clinical trials and investigator-sponsored trials, sharing scientific insights, delivering presentations, and representing the company at selected scientific meetings. The role requires greater than 75% domestic travel, including travel within the territory, to the home office, and to national meetings.

Requirements

Established relationships with HCPs and other KOLs within the territory.
At least 2 years of MSL or Medical Affairs experience.
Solid Tumor focus is required.
Strong knowledge of and/or experience with healthcare and access environments.
Ability to work independently and cross-functionally with numerous internal stakeholders in a highly matrixed environment, including joint-venture collaborations.
Excellent interpersonal, communication, and presentation skills; personal integrity, teamwork abilities, and a customer focus.
Ability to organize, prioritize, and work effectively in a constantly changing environment.
Strong compliance knowledge and adherence to corporate compliance policies.
Current working knowledge of FDA, OIG, ICH, GCP, PhRMA Code, HIPAA, and other compliance regulations and guidelines relevant to industry interactions with healthcare professionals.
Technical acumen, including MS Office skills and ability to adopt and use multiple business applications.
Willingness to travel more than 75% domestically, including within the territory and to the home office and national meetings.

Nice To Haves

Advanced degree, preferably MD, PhD, or PharmD.
At least 5 years of MSL experience.
Experience in Breast Medical Oncology.
Experience with product launches or demonstrated success as a product or therapeutic point of contact.

Responsibilities

Identify key thought leaders and establish, foster, cultivate, and maintain relationships with HCPs in academic and community centers in the assigned territory, including clinical investigators, national and regional opinion leaders, and speakers.
Develop and execute territory plans aligned with U.S. and global Medical Affairs strategies.
Provide insights and feedback on emerging scientific and clinical data to enhance the value and appropriate use of Stemline products through compliant collaboration with internal stakeholders.
Give medical and scientific presentations to internal and external groups.
Respond to unsolicited HCP requests with appropriate clinical and scientific information in a fair and balanced manner.
Liaise with academic research institutions to address medical and scientific inquiries, facilitate investigator-initiated clinical trials, and support company-sponsored clinical trials.
Assist in developing medical communications materials and publications.
Serve as the primary point of contact and facilitator for investigator-sponsored trials, from submission, review, and approval through study activation and completion.
Collaborate with medical and clinical operations teams to support Stemline-sponsored trials through trial-site recommendations and by raising awareness of trials and accrual timelines.
Serve as a scientific resource to commercial partners, as appropriate.
Support the execution, organization, and planning of advisory boards.
Represent Stemline professionally at selected medical and scientific conferences and meetings.
Maintain expertise in therapeutic-area treatment management, new therapies, competitive products, and product features; provide feedback to senior leadership on specific initiatives.
Support safety education for HCPs and allied health professionals regarding use of Stemline products in approved indications.