Medical Scientific Liaison

Baxter International

Newbury, United Kingdom

The Medical Scientific Liaison in Acute for UK, Ireland & the Nordics will provide clinical and technical expertise to the specified Therapeutic Areas (TAs) and will have clinical knowledge for the entirety of the product line(s) related to these TAs. Together with the Regional Medical Director, they are accountable for the implementation of the medical strategy down-stream from Global TA. They are responsible for aligning the Voice of Customer (VOC) with the respective Global Therapeutic Area Leaders and clinical development teams. Critical to this role is the clinical knowledge of therapies and product lines with the ability to offer guidance for product support and product development.

This position, in addition, will work in collaboration with the wider medical affairs team, to align strategic imperatives together with the Regional Medical Director.

This role requires frequent travel within the cluster countries.

What you’ll be doing

Contribute to the development and implementation of the cluster business strategies and tactics.
Provide clinical expertise for the creation, development and delivery of high value-added medical-to-medical educational programs that support commercial team’s efforts.
Deliver medical-to-medical evidence-based presentations and discussions to external medical teams and HCPs to support therapy adoption.
Identify and engage with KOLs and “rising stars” of the respective area of responsibility, establish and maintain peer-to-peer relationships to build awareness, proper use and investigate new uses of the future Vantive products.
Liaison with medical organizations and external subject matter experts within the scope of the Therapeutic Area; e.g. as clinical investigators or scientific consultants.
Responsible for creation and facilitation of scientific Advisory Boards.
Provide scientific support and attendance to conferences and meetings in the respective areas of responsibility.
Review/approve cluster related advertising and promotional, as well as scientific and educational, materials within the therapeutic areas of responsibility.
Provide input into clinical research.
Maintain knowledge base as to developments and trends in medical sciences.
Responsible for cluster medical grant and budgets management in area of TA expertise.
Ensure relevant and appropriate responses to customer medical inquiries.
Be compliant to Ethics, Compliance, internal and external policies.

What you’ll bring

Advanced degree in scientific discipline or equivalent (medical/natural science PhD, MD), with proven clinical experience within the ICU/Intensive care.
Business minded with good strategic awareness thanks to strong medical device/affairs knowledge.
Clinical trial experience with GCP knowledge, and recent teaching/in-servicing to other healthcare professionals is highly desirable.
Excellent medical writing skills proven through successful research experience with literature review, synthesis and analysis.
Strong communication skills and ability to lead public presentations and trainings in applicable GCP and compliance requirements.
Self-motivated and team-oriented with the ability to manage projects and timelines.
Effective critical thinking skills and strategy development.
Excellent skills for building and maintain very good relationships with KOLs/key experts.

Apply Now

Don't forget to mention EuroPharmaJobs when applying.

Share this Job