Senior Manager, Medical Affairs Job at Baxter (Deerfield)

Senior Manager, Medical Affairs

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

United States , Deerfield

Salary:

160000.00 - 220000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Advanced healthcare degree with 8+ years of clinical experience
Background in ICU, Med-Surg, or Clinical Informatics strongly preferred and prior Medical Affairs experience highly desirable
Proven experience within the healthcare or life sciences industry
Strong leadership, interpersonal, analytical, and problem-solving skills
Clinical trial experience with a solid understanding of Good Clinical Practice (GCP)
Working knowledge of biostatistics and clinical trial design
Expertise in literature review, synthesis, and scientific analysis and confidence and effectiveness in public speaking and scientific presentations
Ability to travel up to 50%
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

Provide regional Medical Affairs leadership for new product development, ensuring scientific rigor and clinical relevance
Identify evidence-generation gaps and drive regional evidence strategies in alignment with Global Medical Affairs
Develop and execute scientific communication and non-promotional education plans supporting product and portfolio strategy
Lead and support advisory boards, investigator meetings, roundtables, and scientific forums
Partner cross-functionally to shape long-term Medical Affairs strategies and thought leader engagement plans
Represent Medical Affairs at medical congresses, translating emerging data into actionable insights
Monitor scientific trends and oversee regional activities including grants, sponsorships, and Investigator-Initiated Research
Contribute to clinical and scientific training while building a strong NPE offering for the UCAN HST portfolio
Lead, coach, and develop the Medical Science Liaison (MSL) team
Establish and execute strategies for Key Opinion Leader (KOL) identification, development, and engagement, external engagement metrics and performance excellence, Baxter-funded research (IIRs, BCS, BSS), medical education initiatives and clinical programs.

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

Senior Regional Medical Affairs Manager Center South -Lung Cancer (RMAM)

You will lead regional medical affairs in your area of Germany, building trusted...

Location

Germany , Munich

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Advanced degree in medicine, pharmacy, life sciences or related field (MD, PharmD, PhD or equivalent)
Minimum 3 years ideally experience in medical affairs, medical science liaison, clinical research in lung cancer
Strong clinical and scientific knowledge relevant to the therapy area
Excellent verbal and written communication skills in German and English
Willingness and ability to travel regularly within the assigned region
Solid understanding of regulatory, ethical and compliance requirements in the pharmaceutical environment.

Job Responsibility

Build and maintain scientific relationships with healthcare professionals and external clinical experts in the region
Deliver evidence-based medical education and scientific exchange in person and using digital channels for the area lung cancer
Respond to medical and scientific enquiries from healthcare professionals in a timely and compliant way
Support clinical research collaborations, including identifying study centres and enabling investigator-initiated research
Capture, synthesize and share local clinical insights to inform medical strategy and cross-functional planning
Plan and run regional medical activities such as advisory boards, symposia and educational meetings.

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes.

Fulltime

Senior Manager, Global Medical Affairs (Uterine Health)

We are seeking a highly motivated and experienced Senior Manager, Global Medical...

Location

United Kingdom , London

Salary:

Not provided

Theramex

Expiration Date

Until further notice

Requirements

Medical degree with GMC registration or equivalent international qualification or Master of Pharmacy with GPhC registration
Previous experience in Medical Affairs, Clinical Research, or Pharmacovigilance within the pharmaceutical industry
Very good understanding of Medical Affairs' role as scientific enabler and strategic partner in a pharmaceutical company
Strong knowledge and subject matter in women's health
Ability to cut through scientific complexity and to communicate precisely and clearly with different target audiences
Strong interpersonal and leadership skills and track record of expertise working in a cross-functional environment
Strong analytical and strategic thinking
Strong business acumen
Highest professional work ethics
Proven knowledge of the ABPI Code of Practice and codes of international associations of the pharmaceutical industry, with experience in reviewing and/or certifying materials.

Job Responsibility

Develop and implement medical plans aligned with business objectives and manage associated budgets
Provide expert medical input across the product lifecycle including evidence generation, evidence dissemination (e.g. health care professional education programs), and medical experts’ engagement programs (e.g. advisory boards)
Build and maintain relationships with international therapy area experts and medical-scientific professional societies
Act as a medical reviewer for promotional and non-promotional materials in line with the ABPI and international associations of the pharmaceutical industry codes as well as internal SOPs
Support regulatory and market access submissions with clinical content
Ensure compliance with all relevant regulations and contribute to continuous process improvement
Ensure operational excellence.

Fulltime

Regulatory Affairs Senior Manager – Obesity and Related Conditions

Amgen is seeking a United States Regulatory Lead (USRL) supporting products in t...

Location

United States , Remote; Deerfield; Washington D.C.

Salary:

142579.00 - 192901.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of regulatory experience
Master’s degree and 4 years of regulatory experience
Bachelor’s degree and 6 years of regulatory experience
Associate’s degree and 10 years of regulatory experience
High school diploma / GED and 12 years of regulatory experience
Demonstrated experience with U.S. regulatory submissions and direct FDA interaction, with strong knowledge of the U.S. regulatory environment and drug development lifecycle
Experience contributing to regulatory strategy, including risk assessment, scenario planning, and Health Authority engagement in partnership with global leadership.

Job Responsibility

Contribute to the development and refinement of global regulatory strategy in partnership with the GRL, providing U.S.-specific insights on regulatory precedent, risk, and Health Authority expectations in obesity and related metabolic conditions
Apply scientific expertise in obesity and metabolic disease to inform regulatory strategy, including clinical endpoints and long-term safety considerations
Partner with the GRL and key market leads to align on global development timelines, core documents (e.g., protocols, IBs, KDEs), and regulatory positioning
Execute the U.S. regulatory strategy for assigned programs and represent the region on global governance teams
Plan and lead U.S. regulatory submissions (e.g., clinical trial and marketing applications) in alignment with global filing plans and regulatory requirements
Lead development of key regulatory documents, including labels, briefing packages, and submission components aligned with product strategy
Drive U.S. labeling strategy and execution in collaboration with the Labeling Working Group, including negotiation approach, timelines, and deviation/waiver decisions
Provide strategic input on U.S. development pathways (e.g., expedited programs, orphan designation, pediatric strategy), informed by the evolving regulatory landscape
Lead Health Authority interactions for assigned products, including preparing and leading engagements and communicating outcomes to the GRT and senior management
Manage responses to agency questions (RTQs) and feedback by coordinating cross-functional input and ensuring timely, high-quality submissions

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Corporate Affairs Senior Manager

We are seeking a dynamic and experienced Senior Manager of Corporate Affairs to ...

Location

Japan , Tokyo

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree and 6 years of Communications and/or Advocacy experience
Bachelor’s degree and 4 years of Communications and/or Advocacy experience
Fluent in Japanese and English
Proven experience in corporate communications, public affairs, or public relations or an adjacent field, within healthcare, pharmaceuticals, or biotechnology
Strong ability to understand business priorities and contribute to effective, strategic communication plans
Skilled at translating complex topics into creative yet compliant storytelling that aligns with commercial and corporate goals
Demonstrated success working in a multinational, matrixed organization, leading through influence and aligning diverse stakeholders
Proven ability to work cross-culturally across JAPAC and global teams
Understanding and appreciation of Japanese culture, landscape, and stakeholder expectations and communication approaches
Strong interpersonal skills and ability to work collaboratively across teams

Job Responsibility

Develop and deliver impactful product communications for launches of new medicines and expanded indications
Execute integrated communications strategies across media, emerging media, social and digital media to support corporate priorities, therapeutic areas, and key brand milestones and opportunities
Contribute to strengthening Amgen K.K.’s reputation through clear and authentic storytelling that resonates with key audiences across Japan
Develop and lead an advocacy engagement strategy that fosters trusted relationships with patient advocacy groups, to amplify the patient voice and support improved access to care
Drive disease and patient education communications in partnership with the Brand team including Marketing, Medical, and Value and Access functions
Collaborate with cross-functional partners, including Commercial, Government Affairs, Medical, Legal, Regulatory, to deliver communication activities that highlight Amgen’s commitment to innovation and contribution to Japanese society
Support internal communication efforts to help foster a connected, energized employee culture
Leverage generative AI and analytics tools to elevate quality, speed, and personalization of communications, improve working efficiency, and unlock actionable insights that inform strategies and optimizations
Coordinate best practices and learnings with colleagues in the JAPAC region and the Global Corporate Affairs team
Oversee vendors, when appropriate, ensuring high-quality execution, compliance, and budget discipline

Fulltime

Senior Medical Affairs Advisor, Vaccines

Reporting to the Medical Director, you will provide scientific and medical suppo...

Location

Hong Kong , Quarry Bay

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Bachelor’s degree in pharmacy, pharmacology or other relevant disciplines
Professional experience in hospitals, research or pharmaceutical industry is desirable
Project and process management: ability to manage projects and cross-functional Processes
Administrative excellence: attention to detail evident in a disciplined approach to document training, adherence to SOPs, forecast to spend tracking, metrics, etc.
Organizational skills and able to work independently
Fluent spoken and written English and Chinese

Job Responsibility

Develop, lead and execute the medical strategy, tactics, and operating plan at country level for Vaccines portfolio that fully aligned with the Global, Regional and Local overall strategy goals
Prepare new product launch by generating medical insights and understand the unmet medical needs through medical-to-medical communication, advisory board and data generation
Manage investigator-initiated trial including discussion of research concept with interested researcher, coordinate internal submission and approval of study protocol, and act as a liaison between Pfizer and the researcher
Review promotional materials and customer engagement programs for scientific accuracy and adherence to the relevant policies, guidelines, local industry codes and regulatory guidelines as required
Provide disease and product training to sales and marketing colleagues when required
Establish partnership with patient organizations, professional organizations, medical societies to understand the unmet medical needs. Identify potential ways to address them with an aim to improve patients’ outcomes
Organize medical meetings and activities with KOLs to deliver cutting edge medical information of defined therapeutic area and assigned products
Conduct medical educational meetings to introduce new concepts to help HCPs to improve patients’ outcome and advance their research capability
May speak at medical communication meetings at national and regional levels

Fulltime

New

Senior Director, Medical Affairs Data Analytics and Insights

Join the team transforming care for people with immune challenges, rare diseases...

Location

United States , Morristown; Cambridge

Salary:

206250.00 - 297916.66 USD / Year

Sanofi

Expiration Date

September 28, 2026

Requirements

Advanced degree in healthcare, data science, or related field (PhD, MD, PharmD, or equivalent required)
Masters in data analytics, biostatistics, or related field (valuable, not required)
10+ years of experience in healthcare analytics, with at least 5 years in pharmaceutical industry
Demonstrated expertise in advanced analytics, data science methodologies, and visualization tools
Strong understanding of medical affairs functions and pharmaceutical industry landscape
Experience leading analytics teams and managing complex, cross-functional projects
Deep knowledge of healthcare data sources, RWE, and clinical data analytics
Proven track record of translating complex analyses into actionable insights for stakeholders
Strong business acumen and ability to align analytics strategy with organizational objectives
Experience with modern analytics platforms, visualization tools, and vendors (e.g., Tableau, Power BI)

Job Responsibility

Lead the development and implementation of a comprehensive medical data analytics strategy aligned with business and organizational objectives
Drive the design and execution of advanced analytics solutions to generate impactful medical insights from diverse data sources (RWD, clinical trials, scientific engagement data, medical information)
Establish and oversee the medical data analytics center of excellence, providing strategic direction on analytics methodologies, tools, and capabilities
Partner with cross-functional teams to identify opportunities for data-driven decision making in medical strategy and operations
Lead the evaluation and implementation of innovative analytics technologies, including AI/ML solutions for medical affairs applications
Develop frameworks for measuring and communicating the impact of medical affairs activities through data-driven approaches, including medical care gaps
Provide strategic input into Sanofi's data asset strategy, representing the needs of NA medical therapeutic areas
Serve as an expert consultant to NA medical teams on appropriate use of data assets and platforms
Ensure compliance with data governance, privacy regulations, and industry standards
Build and mentor a team of data scientists and analysts to support medical affairs analytics needs

What we offer

high-quality healthcare
prevention and wellness programs
at least 14 weeks' gender-neutral parental leave

Fulltime

Senior Manager Regulatory Affairs CZ&SK

Senior Manager Regulatory Affairs CZ&SK. Czech Republic - Prague. SALARY RANGE: ...

Location

Czech Republic , Prague

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of directly related experience OR Master’s degree and 6 years of directly related experience OR Bachelor’s degree and 8 years of directly related experience
Degree and in-depth regulatory experience and/or related to the affiliate
Depth knowledge of affiliate legislation and regulations relating to medicinal products
English and Czech and/or Slovak language working proficiency
Good negotiation and Influencing skills
Ability to anticipate and prevent potential issues
Ability to resolve conflicts and develop a course of action leading to a beneficial outcome
Cultural awareness and sensitivity to achieve results across both regional, affiliate and international borders
Ability to manage multiple activities and set priorities
Ability to lead teams and develop effective teams

Job Responsibility

Provides affiliate regulatory expertise and execution for the development, registration, and lifecycle management of all Amgen molecules
Oversee the affiliate and manage a regulatory team to ensure delivery of assigned local and ELMAC Regulatory initiatives
First point of contact for interactions with local regulatory agency(ies)
Ensure that the local Regulatory staff delivers assigned local and ELMAC Regulatory initiatives across the affiliates
Represent Regulatory on the affiliate leadership team
Provide local regulatory input to support development and execution of assigned Regulatory Affairs initiatives and effective interactions with key regulatory agency(ies)
Supervise and oversight for one or more regulatory staff
Manage and liaising with distributors (if applicable)
Translates assigned global, regional and ELMAC Regulatory initiatives into local regulatory objectives where applicable
Acts as senior point of contact for local regulatory advice on commercial and medical activities within the affiliate

Fulltime

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Senior Manager, Medical Affairs

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