Medical Liaison Specialist

2 days ago


Mississauga, Ontario, Canada Baxter Full time

About Baxter

Baxter is a leading global healthcare company that creates innovative medical solutions that transform healthcare. Our mission is to save and sustain lives, and we're committed to making a positive impact on people around the world.

Your Role at Baxter

As a Principal Medical Liaison, you will be a key member of our Medical Affairs team, responsible for interacting with the scientific and clinical community, key opinion leaders, researchers, and medical, pharmacy, and nursing educators. You will be the point of contact for clinical investigators seeking investigator-initiated research support and will develop professional relationships with key opinion leaders in key therapeutic areas.

Key Responsibilities

  • Provide remote or on-site Master Drug Library (MDL) software training for MDL administrators on the creation and maintenance of the MDL.
  • Review MDLs created by newly-trained administrators and outline opportunities for improvement as necessary.
  • Participate in on-site MDL vetting and testing sessions with key stakeholders at the institution.
  • Provide remote or on-site training on continuous quality improvement reports for all new MDL administrators.
  • Identify resource requirements and schedule those resources as required to ensure safe and efficient implementations and successful evaluations.
  • Provide remote or on-site ongoing clinical support and/or supplemental training for MDL administrators or other account representatives requesting assistance with drug library needs or issues.
  • Identify, establish, and maintain scientific peer-to-peer relationships with Key Opinion Leaders (KOLs) and healthcare professionals.
  • Attend and provide scientific support at R&D exhibits and scientific sessions at regional, national, and international medical conferences.
  • Support advisory boards, clinical investigator meetings, educational forums, and organize and chair roundtable and educational meetings as needed.
  • Identify and communicate new scientific findings and opportunities or threats that could impact the portfolio.
  • Provide medical and scientific support of our strategy of health outcomes, real-world evidence, and payer/provider engagements.
  • Collaborate with business partners to develop long-term strategic plans, including comprehensive thought leader plans.
  • Support the management of Grants, including acting as the primary liaison to investigators interested in developing and performing Investigator-Initiated Research (IIR) grants.
  • Provide medical support to Regulatory Affairs, Quality, Medical Information, Health Economics and Outcomes Research, and other functions as needed.

Requirements

  • Pharmacist professional degree with at least 5 years of clinical pharmacy experience.
  • An active Canadian pharmacist license in good standing.
  • Bilingual in English and French is required.
  • Travel will be required and will involve a minimum of 40% nationally in Canada.
  • Knowledge of medication safety principles and their application to smart infusion pumps.
  • Demonstrated understanding of intravenous drug dosing and administration.
  • Experience in reporting of adverse events with basic knowledge of biostatistics and trial design.
  • Computer literacy and PowerPoint skills, relationship building, and experience presenting medical education.
  • Experience with literature review and interpretation.
  • Must be able to work independently and within groups in a collegial manner.

Nice to Have

  • Minimum 5 years of Canadian acute care hospital experience with pharmacy operations experience preferred.
  • Demonstrated understanding of drug library building, vetting, and maintenance is preferred.
  • Demonstrated knowledge of smart pump implementation is preferred.
  • Industry experience is preferred.
  • Health outcomes experience is preferred.


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