Sr. Manager, Medical Affairs

Employment Type: Full time Location Type: Salary:

Position Overview

At Baxter, we are deeply connected by our mission to save and sustain lives. Our work makes a positive impact on people worldwide, providing a sense of purpose as our products and therapies are found in hospitals, clinics, and homes globally. For over 85 years, Baxter has pioneered significant medical innovations. We foster a collaborative environment where employees are happy, successful, and inspire each other. Join us at the intersection of saving and sustaining lives, where your purpose accelerates our mission.

Your Role at Baxter

Your work as a Sr. Manager, Medical Affairs contributes directly to making a significant impact on others by improving patient outcomes through the research and products we develop. This challenging role involves cross-functional collaboration and leading by influence, whether guiding a team through a project or leading direct reports. Our research and development team is responsible for influencing others to achieve results.

Your Team

While everyone at Baxter shares a passion for our mission, this role is critical to our ability to save and sustain lives. We encourage teamwork and collaboration, prioritizing the building of relationships based on reliability, ethics, and care. We rely on our colleagues' expertise and hold each other accountable.

Responsibilities

As the Sr. Manager, Medical Affairs, you will provide clinical/technical expertise to Baxter’s Global Infusion Systems and Patient Monitoring business unit, covering the entirety of the related portfolio. Key to this role is clinical knowledge of infusion practices, hemodynamic patient monitoring, and IV fluid management, with the ability to offer guidance for product support and development.

• Provide high-quality, evidence-based medical and scientific information upon request internally (e.g., Clinical Development, Marketing, Manufacturing, Quality Assurance, Regulatory Affairs, R&D, Legal) and externally.
• Maintain current familiarity with relevant published medical literature to provide information relating to clinical trends and potential impacts on product lines.
• Develop a basic understanding and maintain current knowledge of regulatory/quality requirements related to R&D and product support.
• Support Regulatory Affairs and Quality teams by providing clinical input into the evaluation of product complaints/adverse events.
• Provide clinical expertise for the creation, development, and/or execution of training programs supporting sales and marketing efforts.
• Help manage and support global medical activities such as publications, advisory boards, clinical investigator meetings, and educational forums.
• Provide medical and scientific expertise in assessing and interpreting publications and data.
• Translate scientific knowledge to support medical and commercial activities within the business unit.
• Use scientific evidence to evaluate and substantiate advertising and promotional claims.
• Develop and maintain peer-to-peer collaborations and relationships with medical and scientific experts.
• Serve as the medical affairs subject matter expert for sustaining product activities.
• Collaborate cross-functionally with global and regional Medical Affairs and Commercial teams.
• Represent the global business unit in internal and external meetings as requested.
• Possess excellent medical writing and presentation skills.

Requirements

• Clinically skilled, licensed health care professional, preferably a Registered Nurse (RN) with experience in Critical Care.
• 8+ years of clinical experience.
• Experience within