Principal Medical Science Liaison Job at Baxter (Deerfield)

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Principal Medical Science Liaison - Smart Infusion Pumps

The Medical Science Liaison (MSL) is a field-based member of the US Medical Affa...

Location

United States , Deerfield

Salary:

128000.00 - 176000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Pharmacist or nurse professional degree with at least 5 years of hospital pharmacy or nursing experience
Demonstrated understanding or experience using smart infusion pumps
Experience with literature review and interpretation
Experience presenting medical education
Experience in reporting adverse events with basic knowledge of biostatistics and trial design
Ability to work independently and within groups in a collegial manner
Must have presentation skills
Travel will be required and will involve a minimum of 70% nationally within Western United States
Applicants must be authorized to work for any employer in the U.S.
We are unable to sponsor or take over sponsorship of an employment visa at this time

Job Responsibility

Identify, establish, and maintain scientific peer-to-peer relationships with Key Opinion Leaders (KOLs) and health care professionals, by partnering with them on scientific projects, presenting balanced scientific data, crafting sophisticated educational forums and providing scientific support in the development of clinical publications
Attend and provide scientific support 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 as well as medical affairs 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

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence
Paid parental leave
Commuting benefits

Fulltime

Principal Medical Science Liaison - Smart Infusion Pumps

The Medical Science Liaison (MSL) is a field-based member of the US Medical Affa...

Location

United States , Deerfield

Salary:

128000.00 - 176000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Pharmacist or nurse professional degree with at least 5 years of hospital pharmacy or nursing experience
Demonstrated understanding or experience using smart infusion pumps
Experience with literature review and interpretation
Experience presenting medical education
Experience in reporting adverse events with basic knowledge of biostatistics and trial design
Ability to work independently and within groups in a collegial manner
Must have presentation skills
Travel will be required and will involve a minimum of 70% nationally within Western United States

Job Responsibility

Identify, establish, and maintain scientific peer-to-peer relationships with Key Opinion Leaders (KOLs) and health care professionals, by partnering with them on scientific projects, presenting balanced scientific data, crafting sophisticated educational forums and providing scientific support in the development of clinical publications in accordance with company policies, applicable laws, regulations and ethical standards
Attend and provide scientific support 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 as well as medical affairs 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

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence
Paid parental leave

Fulltime

Principal Medical Science Liaison

The Principal Medical Science Liaison (MSL) is a senior, field-based Medical Aff...

Location

United States , Deerfield

Salary:

128000.00 - 176000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Physician Associate (PA) or Physician (MD/DO) required with a minimum of 3 years of surgical experience in an operating room environment
Ability to travel 70% within the Central U.S.
MD/DO with board certification in Cardiac, Spine, Gynecologic, or General Surgery
5+ years of experience in Medical Affairs, medical device, or pharmaceutical industry
Prior experience operating at a principal MSL level, including regional strategy influence
Demonstrated ability to build credibility rapidly with surgeons and OR teams
Deep understanding of Medical Affairs Code of Practice and industry compliance standards
Working knowledge of regulatory and clinical research requirements, including IIR processes
Exceptional communication and presentation skills
High ethical standards, professionalism, and scientific rigor

Job Responsibility

Serve as the senior medical expert for Advanced Surgery technologies, including hemostats, sealants, tissue repair, and emerging surgical innovations
Lead peer-to-peer scientific exchange with surgeons and interdisciplinary healthcare professionals in Cardiac, Spine, Gynecologic, and General Surgery
Translate complex clinical, surgical, and health economic data into actionable medical insights to optimize patient outcomes
Develop and sustain trusted relationships with national, regional, and emerging Surgeon KOLs
Identify, cultivate, and support investigators for Investigator-Initiated Research (IIR) and Baxter-sponsored studies
Capture and communicate voice-of-customer insights to influence clinical evidence strategy and innovation pipelines
Contribute to and help execute regional Medical Affairs strategies, including real-world evidence (RWE) generation and publication planning
Support advisory boards, investigator meetings, and scientific panels
Partner with global and regional teams to support clinical trial feasibility, site identification, and execution
Design and deliver high-impact medical education, including: Medical congress presentations Company-sponsored symposia, Surgical training labs, and mobile lab programs Resident, fellow, and nurse education initiatives

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
Commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)

Fulltime

Principal Medical Science Liaison - Smart Infusion Pumps

The Medical Science Liaison (MSL) is a field-based member of the US Medical Affa...

Location

United States , Deerfield

Salary:

128000.00 - 176000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Pharmacist or nurse professional degree with at least 5 years of hospital pharmacy or nursing experience
Demonstrated understanding or experience using smart infusion pumps
Experience with literature review and interpretation
Experience presenting medical education
Experience in reporting adverse events with basic knowledge of biostatistics and trial design
Ability to work independently and within groups in a collegial manner
Must have presentation skills
Travel will be required and will involve a minimum of 70% nationally within Western United States

Job Responsibility

Identify, establish, and maintain scientific peer-to-peer relationships with Key Opinion Leaders (KOLs) and health care professionals
Attend and provide scientific support 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 as well as medical affairs 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

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts
Educational assistance programs
Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence
Paid parental leave
Commuting benefits

Fulltime

Principal Medical Science Liaison

The Principal Medical Science Liaison (MSL) is a senior, field-based Medical Aff...

Location

United States , Deerfield

Salary:

128000.00 - 176000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Physician Associate (PA) or Physician (MD/DO) required with a minimum of 3 years of surgical experience in an operating room environment
Ability to travel 70% within the Central U.S.

Job Responsibility

Serve as the senior medical expert for Advanced Surgery technologies
Lead peer-to-peer scientific exchange with surgeons and healthcare professionals
Translate complex clinical data into actionable medical insights
Develop and sustain trusted relationships with Surgeon KOLs
Identify and support investigators for Investigator-Initiated Research
Capture voice-of-customer insights
Contribute to regional Medical Affairs strategies
Support advisory boards, investigator meetings, and scientific panels
Design and deliver high-impact medical education
Review promotional and non-promotional materials

What we offer

Medical and dental coverage that start on day one
Basic life, accident, short-term and long-term disability insurance
Business travel accident insurance
Employee Stock Purchase Plan (ESPP) with ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP) with employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence

Fulltime

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States , Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Excellent attention to detail
Good written and verbal communication skills
Good collaboration and interpersonal skills
Good negotiation skills
Proficient in written and spoken English language required
Fluency in local language(s) required
Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP
Good knowledge of relevant local regulations
Good medical knowledge and ability to learn relevant Client Therapeutic Areas
Basic understanding of the drug development process

Job Responsibility

Contributes to the selection of potential investigators
In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance
Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles
Confirms that site staff have completed and documented the required training appropriately
Actively participates in Local Study Team (LST) meetings
Contributes to National Investigators meetings, as applicable
Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
Shares information on patient recruitment and study site progress (site quality/performance) within the LST
Drives performance at the sites
Updates CTMS and other systems with data from study sites as per required timelines

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Fulltime

Senior Clinical Materials Project Manager

Leads or coordinates cross-functional project/program teams from design to deliv...

Location

United States of America , Rochester

Salary:

63815.00 - 95723.00 USD / Year

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor’s Degree with major course works in appropriate health, social science, or biological science field required
Minimum 5-10 years of experience, or equivalent combination of education and experience required
Clinical trials project management experience preferred
Knowledge of Good Manufacturing Practices and Good Clinical Practices, planning, implementation, and coordination of clinical trials
Strong communication skills, including written communication
Strong presentation, interpersonal and organizational skills, and attention to detail
Travel required (up to 5%)

Job Responsibility

Leads or coordinates cross-functional project/program teams from design to delivery of fully-developed products that are ready for customer use
Monitors performance and recommends schedule changes, cost adjustments or resource additions
Investigates facts and develops solutions to problems during the design and planning phases
Provides timely and accurate information and status updates to functional leaders
May be responsible for feasibility studies, field trials management, identifying product gaps, defining product requirements and engaging with customers to understand market needs and trends
Directs and oversees the planning, implementation, coordination, and supply chain of clinical supplies to support multi-center clinical trials
Plans internal meetings and provides professional direction within the clinical materials service unit team
Develop and deliver training programs to support new processes and projects
Serves as liaison to study sponsors, clinical coordinating centers, data coordinating centers, clinical trial sites, pharmacy departments, contract research organizations, study principal investigators, study medical monitors, biostatistics department, and administration/fiscal unit
Drafts and develops the CMSU’s Clinical Materials Specifications Sheet (CMSS), processing orders, shipping instructions, packing lists/Acknowledgement of Receipts (AOR’s), and study drug handling instructions

Fulltime

Project Manager II, Learning Health Systems

Under administrative review, performs management level work directed toward the ...

Location

United States , Winston Salem

Salary:

33.05 - 49.60 USD / Hour

Advocate Health Care

Expiration Date

Until further notice

Requirements

Master's degree in Psychology, Nursing, or Basic Science with two years' relevant administrative and medical experience in research projects or other health-related activities
or, an equivalent combination of education and experience.
One-year experience in a supervisory capacity.
Excellent oral and written communication skills
Demonstrates knowledge of scientific principles
Experience in both single- and multi-center studies

Job Responsibility

Oversees the operational activities at the clinical site(s) and coordinates the activities of a multi-center study or multiple large studies.
Collaborates with principal investigator(s) in developing plans for research projects and to discuss the interpretation of results. Negotiates protocol changes with funding agency/sponsor.
Assumes major responsibility for the successful and timely completion of the tasks that comprise the implementation and analysis phases of a multi-center study or multiple studies including planning, development, implementation, and evaluation.
Coordinates the hiring of and provides direction to support staff. Plans and coordinates training sessions for project personnel located at the different clinical sites. Oversees recruitment, data collection, and follow-up activities.
Translates planning and design decisions into concrete activities and tasks for project implementation, and sets priorities for project implementation.
Evaluates and interprets collected clinical data. Manages the preparation of progress reports and quality control monitoring
participate in the analysis of study data and the writing of scientific papers for publication.
Develops data collection forms, procedural manuals, and other documents required for project implementation and evaluation.
Ensures that all aspects of the following are completed: a. Study is conducted in accordance to the study protocol and contract b. Legal aspects adhere to state and federal regulations and guidelines c. Requirements of the Medical School and the University comply with the conduct of the study d. Technical requirements of the funding agency are met, including auditing requirements
Conducts site visits to evaluate staff and study activities. Coordinates sponsor audits.

What we offer

Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program

Fulltime

Principal Medical Science Liaison

Baxter

Location:
United States , Deerfield

Category:
IT - Software Development

Contract Type:
Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
May 03, 2026

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Principal Medical Science Liaison

Baxter

Location:United States , Deerfield

Category:IT - Software Development

Contract Type:Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:May 03, 2026

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Job Posted:
May 03, 2026