Medical Science Liaison Gynecology Oncology Expert

hace 2 semanas

Buenos Aires, Buenos Aires C.F., Argentina AbbVie A tiempo completo
Job Summary:

At AbbVie, we are seeking a highly skilled Medical Science Liaison to join our team in supporting the medical and scientific objectives of our pharmaceutical company. The ideal candidate will have a strong background in Gynecologic Oncology and demonstrate expertise in the scientific methods applied to clinical research, as well as current legislative and regulatory controls applicable to this research.

Key Responsibilities:
  • Represent AbbVie Medical Affairs as a subject matter expert in the assigned therapeutic area and territory, providing scientific and technical leadership to ensure professional and credible relationships with external experts/HCPs of strategic importance to AbbVie.
  • Serve as a point of contact within the Medical Affairs team for external experts within an assigned geographic area to satisfy their needs for scientific knowledge in a therapeutic area and, when requested, relevant AbbVie medicines, to support their safe, effective, and appropriate use.
  • Develop and execute scientific interaction plans, cycle plans; contribute to cross-functional account planning, as appropriate.
  • Responsible for appropriate tiering and segmentation of external experts based on guidance from the IFT playbooks and appropriate documentation of HCP interactions and relevant insights in the CRS and related platforms and systems.
  • Ensure a strong medical and scientific presence for AbbVie in key academic centers by facilitating research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic interest to AbbVie.
  • Support internal teams such as sales and marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations. Work collaboratively and cross-functionally with other in-field members while retaining functional independence.
  • Assist in the initiation, oversight, and follow-up of assigned GMA studies and medical projects initiated within the therapeutic area for which the MSL carries responsibility (e.g., registry/database projects, epidemiological studies, post-authorization studies).
  • Support prioritized interventional studies run by Clinical Development Operations, with study initiation visits and act as subject matter expert as part of One R&D community. All such activities must comply with applicable local laws, guidelines, codes of practice, SOPs, and AbbVie R&D SOPs.
  • Act as the point of contact with external experts to facilitate investigator-initiated study (IIS) ideas and requests for support to the local and global medical teams as appropriate.
  • Deliver credible presentations on scientific matters to physicians, individually or in groups (meetings, clinical sessions, etc.), where requested, but with the focus on thought leaders.
  • Attend relevant scientific meetings and Conferences. Collaborate with internal stakeholders to develop summaries of key data and other scientifically relevant information to inform AbbVie strategic priorities and initiatives.
  • Upon request, assist physicians with requests for access to AbbVie medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory requirements.
  • Provide key thought leaders/external experts and internal medical and clinical teams with scientific and technical support for publications of scientific or medical interest.
  • Ensure that all activities and interactions are conducted with due regard to all applicable local, global, and national laws, regulations, guidelines, codes of conduct, Company policies, and accepted standards of best practice.
Requirements:
  • Advanced degree (e.g., PharmD., MD, PhD) in a relevant scientific discipline is preferred (Gyneco-Oncology) but candidates with an undergraduate degree in a relevant discipline and demonstrated experience will be considered, more than 3 years of experience in developing and maintaining expert knowledge for the assigned therapeutic area, and in medical research in general.
  • Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company.
  • Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research.
  • Ability to comprehensively learn about new subject areas and environments.
  • Excellent written and spoken communication and presentation skills, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians, and other healthcare decision makers.
  • A good understanding of written and oral English is desirable.
  • High customer orientation.
  • Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity.
  • Experience in solid tumors.

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