Gastroenterology Medical Expert

hace 4 días

Buenos Aires, Buenos Aires C.F., Argentina Allergan A tiempo completo

Company Overview



Our company is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.



The Role

We are seeking an experienced Medical Science Liaison (MSL) to join our team in the Gastroenterology therapeutic area. The successful candidate will be responsible for representing the company as a subject matter expert, providing scientific and technical leadership, and ensuring professional and credible relationships with external experts/healthcare professionals of strategic importance.



Key Responsibilities


  • Represent the company as a subject matter expert in the assigned therapeutic area, providing scientific and technical leadership to ensure professional and credible relationships with external experts/healthcare professionals of strategic importance.
  • Serve as a point of contact within the Medical Affairs team for external experts within an assigned geographic area, satisfying their needs for scientific knowledge in a therapeutic area and, when requested, relevant company 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 internal playbooks and documentation of HCP interactions and relevant insights in the CRS and related platforms and systems.
  • Ensure a strong medical and scientific presence for the company in key academic centers by facilitation of research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic interest to the company.
  • 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 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 a 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 company R&D SOPs.
  • Act as the point of contact with external experts to facilitate investigator-initiated study 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 a 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 company strategic priorities and initiatives.
  • Upon request, assist physicians with requests for access to company 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.

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