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Secura Bio

Commercializes oncology therapies and develops COPIKTRA

Medical Science Liaison

Biology & BiotechUpdated on Nov 14
Full-timeRemote in USA$196k - $239k

About the Job

Requirements

  • An advanced degree is strongly preferred; candidates with an MBA or MSc require 5+ years of relevant experience, while BA/BSc candidates require 8+ years. Clinically licensed professionals (NP, PA, RN) may be considered with substantial oncology or Medical Affairs experience.
  • At least 3 years of experience in Medical Affairs, field medical, pharmaceutical, or biotech roles, demonstrating maturity in scientific exchange and territory leadership.
  • Strong subject matter expertise in oncology or hematology, including experience supporting product launches, understanding treatment paradigms, clinical pathways, and emerging research trends.
  • Deep understanding of cancer biology, mechanisms of action, and therapeutic modalities relevant to rare lymphomas.
  • Ability to communicate complex scientific information to oncologists, researchers, and multidisciplinary stakeholders.
  • Capability to deliver scientific presentations to audiences of varying sizes with clarity and confidence.
  • Experience analyzing complex clinical trial data and translating findings into clinically meaningful insights.
  • Experience engaging and building trust with key opinion leaders in oncology.
  • Understanding of drug development, regulatory pathways, and how field insights shape clinical strategy.
  • Knowledge of oncology practice patterns, care delivery models, and healthcare system dynamics.
  • Ability to identify clinical research opportunities, evaluate investigator potential, and support collaborative scientific initiatives.
  • Ability to collaborate effectively with colleagues in clinical development, clinical operations, commercial, and Medical Affairs.
  • Ability to work independently and deliver results in a fast-paced environment.
  • Adaptability to evolving scientific data, shifting priorities, and the fast-paced environment of a small oncology company.
  • Familiarity with pharmaceutical and biotech compliance guidelines governing scientific exchange and field medical activities.

Responsibilities

  • Identify, cultivate, and sustain high-value relationships with key opinion leaders and healthcare professionals across the territory, and communicate scientific data, research concepts, and educational content about the company’s products and therapeutic focus.
  • Set territory medical priorities, anticipate needs, and drive aligned activities that support Medical Affairs objectives.
  • Deliver balanced, scientifically rigorous information about pipeline and marketed products to internal and external stakeholders.
  • Gather, synthesize, and communicate actionable field insights to inform medical strategy, clinical development, and cross-functional decision-making.
  • Serve as a scientific resource during medical congresses, advisory boards, training programs, mentorship activities, and strategic planning meetings.
  • Collaborate with Clinical Development and Operations on sponsored research initiatives, including site identification and evaluation, recruitment support, investigator engagement, external expert identification, and management of scientific collaborations.
  • Facilitate submission and review of investigator-initiated research proposals, maintain communication with investigators, and support company-sponsored research activities.
  • Partner with Market Development Managers and Key Account Managers to provide scientific education, customer support, and territory planning aligned with medical objectives and broader business goals, as appropriate.
  • Contribute to regional and national Medical Affairs strategies through territory medical planning, post-congress insight generation, and identification of emerging scientific trends.
  • Adopt and use digital technologies and resources to enhance scientific exchange, insight capture, and field effectiveness.

Desired Qualifications

  • Background in hematologic malignancies, especially lymphoma.
  • Flexibility to travel 60–80% of the time.
  • Attendance at major oncology conferences such as ASCO, ASH, and SOHO, as well as regional conferences.
  • Must reside within IL, ND, SD, NE, MO, IA, MN, or WI, with preference for major metropolitan areas in IL, MN, or MO.
  • Willingness and flexibility to travel occasionally on weekends for meetings and conferences.
  • Valid driver's license and good driving record.

About the Company

Secura Bio

Commercializes oncology therapies and develops COPIKTRA

Secura Bio is an integrated biopharmaceutical company focused on bringing oncology therapies to patients. Its main product is COPIKTRA (duvelisib), an oral PI3K inhibitor used to treat adults with relapsed or refractory chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL). The company is also running a Phase 3 study of COPIKTRA for relapsed or refractory nodal T-follicular helper cell lymphoma. Secura Bio’s approach centers on acquiring, developing, and commercializing approved and late-stage oncology assets, with headquarters in Las Vegas and a European office in Dublin. In simple terms, the company buys or develops cancer drugs and then brings them to doctors and patients who need them. Its goal is to close the gap between available oncology therapies and the patients who can benefit from them.

Company size
51-200
Company stage
Late Stage VC
Total funding
$55M
Headquarters
Berkeley Heights, NJ
Founded
2019

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