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Medical Science Liaison-Solid Tumor (New England)

Menarini Group

United States

Remote

USD 90,000 - 150,000

Full time

30+ days ago

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Job summary

An established industry player is seeking a (Sr) Medical Science Liaison for the New England region. This role involves engaging with key opinion leaders and healthcare providers to facilitate scientific discussions and support clinical research initiatives. The ideal candidate will have a strong background in oncology, excellent communication skills, and the ability to work independently in a dynamic environment. Join a forward-thinking company dedicated to innovation and patient care, where your contributions will help shape the future of oncology treatment and research.

Qualifications

  • Advanced degree preferred with experience in Oncology and MSL roles.
  • Strong communication and relationship-building skills are essential.

Responsibilities

  • Cultivate relationships with healthcare providers and key opinion leaders.
  • Provide medical information and support for clinical trials.
  • Represent the company at medical and scientific conferences.

Skills

Interpersonal Communication
Presentation Skills
Oncology Knowledge
Relationship Building
Compliance Knowledge
Project Management
Scientific Exchange

Education

MD
PhD
PharmD

Tools

MS Office

Job description

Overview

Medical Science Liaison-Solid Tumor (New England)

Reports to Regional Director, Solid Tumor MSL

Founded in 1886 in Naples under the name of Farmacia Internazionale, Menarini moved in 1915 to Florence where the Group’s headquarters are still located today. High quality therapeutics and diagnostics solutions for patients, ethics as our underlying principle, dedication to innovation and advancement, strong people centricity and environmental sustainability. These five pillars form the foundation of the Menarini Group, an Italian pharmaceutical company with nearly 135 years of history.

The Menarini Group is present in 140 countries around the world. Its companies span from Europe to Asia, to Africa and the Middle East, to Central America and to the United States where with the acquisition of Stemline Therapeutics, a NASDAQ-listed biopharmaceutical company, the company marked its entry into the US oncology market.

Thanks to the valuable contribution of around 18,000 employees, every year more than 500 million packs of drugs are produced at the Group's 18 manufacturing sites including a biotech plant for the manufacturing of monoclonal antibodies that also serves external clients distributed across 6 continents.

Menarini has made a strong commitment to oncology, investing in a pipeline of five investigational compounds for the treatment of a variety of hematological and solid tumors. The acquisition of Stemline Therapeutics in June 2020, further strengthened Menarini’s oncology portfolio, adding both commercial and clinical-stage assets.

It is an exciting time in the company’s development and an excellent opportunity for individuals joining us to contribute to building and shaping Menarini Stemline’s Oncology business.

Opportunity

Menarini Stemline is hiring a (Sr) Medical Science Liaison for the New England region (MA, ME, VT, NH, RI, CT). The Medical Science Liaison (MSL) will be responsible for the scientific exchange of Stemline’s pipeline, disease state awareness and general scientific discussions of data with Key Opinion Leaders (KOLs) and Health Care Providers (HCPs). The MSL will represent Stemline in the support of research interest with both Company Sponsored Trials and Investigator Initiated Research. MSLs provide medical information through scientific exchange in a fair and balanced manner and provide clinical/scientific support. The MSL will also support the safety education to HCPs and allied health professionals for the use of Stemline products in approved indications.

Responsibilities
  • Identify key thought leaders and establish, foster, cultivate, and maintain relationships with healthcare providers (HCPs) in academic and community centers within assigned territory including but not limited to clinical investigators, national and regional opinion leaders, and speakers.
  • Develop and execute territory plans in alignment with US and global Medical Affairs strategies.
  • Provide insights/feedback on emerging scientific/clinical data that enhance the value and appropriate use of Stemline products as part of compliant collaboration with internal stakeholders.
  • Give medical/scientific presentations to internal and external groups.
  • Present appropriate clinical and scientific information to healthcare providers in response to unsolicited requests (as appropriate) 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 the development of medical communications materials and publications.
  • Act as the primary point of contact and facilitator for all aspects of investigator-sponsored trials (ISTs), from submission, review and approval, through study activation/completion.
  • In collaboration with medical and clinical operations teams, support Stemline-sponsored trials through trial site recommendations and raise awareness of the trials and accrual timelines.
  • Serve as a scientific resource to commercial partners, as appropriate, to support activities.
  • Support the execution, organization, and planning of advisory boards.
  • Professionally represent Stemline at select medical and scientific conferences and meetings.
  • Sustain expertise in therapeutic area treatment management and new therapies, competitive products and features, and provide feedback to the senior leadership team on specific initiatives.
Qualifications
  • Advanced degree preferred: (MD, PhD, PharmD preferred)
  • Established relationships with HCPs and other KOLs within territory.
  • At least 5 years of MSL experience preferred.
  • At least 2 years MSL/Medical Affairs experience in Oncology; Solid Tumor focus preferred.
  • Breast cancer experience is strongly preferred.
  • Strong knowledge and/or experience of healthcare and access environments.
  • Proven ability to work independently, as well as cross-functionally with numerous internal stakeholders in a high-matrixed environment, including joint venture collaborations.
  • Preferred experience on product launches or demonstrated success as product or therapeutic point of contact.
  • Excellent interpersonal communication and presentation skills, strong personal integrity, teamwork abilities, and a customer focus are necessary.
  • Must be able 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.
  • Demonstrated technical acumen including MS Office skills and the ability to adopt and leverage multiple business applications.
  • This position will require greater than 75% domestic travel, including within the territory, and to the home office and national meetings.

Menarini Stemline is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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