CrawlJobs Logo
Cabaletta Bio Inc Logo Cabaletta Bio Inc · IT - Administration

Senior Director, Field Medical Affairs Team Lead

United States · Job Posted May 16, 2026
Apply Position
Job Link Share

Job Description

We are seeking a highly motivated and experienced Senior Director, Field Medical Affairs Team Lead to lead the strategic development, build-out, and execution of the field medical organization in support of rese-cel in myositis and other autoimmune diseases. This leader will play a critical role in shaping field medical strategy, generating scientific insights, and establishing strong relationships with trial investigators, key opinion leaders (KOLs) and cell therapy treatment centers in a highly specialized and evolving therapeutic area. This position requires deep expertise in cell therapy, strong leadership capabilities, and experience in launching cellular therapies, including building teams, developing field strategies, and aligning cross-functional stakeholders.

Job Responsibility

  • Leadership & Team Development
  • Medical Strategy & Execution
  • KOL & External Engagement
  • Cross-Functional Collaboration
  • Pre-Launch & Launch Readiness
  • Operational Excellence

Requirements

  • Advanced scientific degree (PharmD, PhD, MD, DO) with at least 10 years of experience in the pharma/biotech industry
  • Minimum of 8 years' experience as a Medical Science Liaison and 3-5 years leading a team of Medical Science Liaisons within the cell therapy space is required
  • Experience in cell therapy site certifications for commercialization is highly desirable
  • Therapeutic area expertise in immunology or autoimmune diseases is desirable but not required
  • Demonstrated ability to build and maintain relationships with internal and external stakeholders, fostering collaboration and alignment
  • Proven track record of developing and executing medical affairs strategies to support product development, launch, and lifecycle management
  • Experience with developing and implementing KPIs for field engagement
  • Expertise in the use of Customer Relationship Management tools (i.e. Veeva CRM)
  • Excellent communication skills, with the ability to distill complex scientific concepts into clear, concise messages for KOLs and diverse audiences
  • Familiarity with regulatory requirements and ethical standards governing scientific research and development
  • Strategic thinking and problem-solving abilities, with a focus on driving innovation and achieving organizational objectives
  • Must be able to influence in a matrixed environment
  • Flexibility and adaptability to work in a dynamic, fast-paced environment, managing multiple projects simultaneously
  • Remote, field-based role with expected travel ~50% (mostly within US)
  • Must be able to work Eastern Time hours, regardless of location

Nice to have

  • Experience in cell therapy site certifications for commercialization is highly desirable
  • Therapeutic area expertise in immunology or autoimmune diseases is desirable but not required

What we offer

  • health and retirement
  • PTO
  • stock option plans
Cabaletta Bio Inc - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Senior Director, Field Medical Affairs Team Lead

8 matching positions

Senior Director, Field Medical, Southeast

ViiV Healthcare is a global specialty HIV company, the only one that is 100% foc...
Location
Location
United States , Montgomery; Miami; Orlando; Tampa; Atlanta; New Orleans; Charleston
Salary
Salary:
Not provided
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree in medical OR health sciences OR clinical discipline (MD, DO, PharmD, NP, PA)
  • 10 plus years of pharmaceutical experience in medical affairs
  • 5 plus years of field medical experience
  • Matrix leadership experience
  • People Management experience
  • Experience managing Key Stakeholders
  • Experience with regulatory requirements
  • Ability to travel up to 70% of the time
  • Valid Driver's License
Job Responsibility
Job Responsibility
  • Team Leadership and Management: Lead, oversee, coach, mentor and provide guidance to a team of field medical personnel
  • People Leadership and Development: Recruit, develop and retain key talent
  • Strategic Planning & Execution: Accountable for the direction and execution of strategic medical objectives and territory plans
  • Cross-Functional Collaboration: Collaborate with cross-functional business partners to enhance team effectiveness and drive overall team performance
  • Scientific Expertise: Responsible for scientific knowledge and expertise of self and team
  • Scientific Engagement: Ensure the team has a robust interface with external experts, healthcare professionals, and industry experts
  • Business Performance: Analyze and leverage scientific and performance data to provide actionable insights
  • Training and Development: Ensure team is are well-trained with the latest scientific information and core industry compliance standards
  • Compliance and Quality: Responsible for team compliance of all field medical activities with applicable regulatory guidelines and company policies
  • Clinical Trial Support: Lead MSL support of ViiV US sponsored and supported research in specific region
What we offer
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
Read More
Arrow Right

Senior Director, Global Medical Affairs, Oncology

Moderna is seeking a Global Medical Director to lead medical affairs strategy ac...
Location
Location
United States , Cambridge
Salary
Salary:
210900.00 - 379200.00 USD / Year
modernatx.com Logo
Moderna
Expiration Date
July 13, 2026
Flip Icon
Requirements
Requirements
  • MD or non-US equivalent, PharmD, or PhD with extensive oncology medical affairs leadership experience
  • Minimum of 15 years of experience in Medical Affairs, with a strong track record in global roles
  • Demonstrated leadership of global launch planning and execution in oncology or immuno-oncology settings
  • Deep expertise in oncology therapeutic area required
  • Strong strategic thinking and leadership skills in a global medical affairs role
  • Experience in regulatory, scientific communication, and external stakeholder engagement
  • Launch experience global and/or locally
Job Responsibility
Job Responsibility
  • Owning and leading the global medical strategy across Moderna’s oncology portfolio, ensuring seamless integration from early development to lifecycle management
  • Serving as final medical accountability for assigned oncology programs, including delivery of the integrated medical plan
  • Driving medical leadership in governance bodies and cross-functional decision-making forums, ensuring alignment between development, regulatory, and commercial functions
  • Leading the Development Integrated Evidence Team to build comprehensive data packages for regulators, payers, and other stakeholders
  • Acting as global medical lead in interactions with health authorities and payers, providing strategic input and medical representation
  • Directing a cross-functional global medical matrix team (Scientific Communications, Field Medical, Patient Advocacy), ensuring timely execution of deliverables
  • Leading global launch readiness for oncology assets, including medical training, evidence generation, scientific engagement, and narrative development
  • Building partnerships with global, regional, and national thought leaders to shape best practices and influence health policy
  • Developing and executing publication strategies, medical education initiatives, and real-world evidence programs to strengthen knowledge exchange
  • Managing medical affairs budget and resource planning for assigned programs, aligning with broader franchise objectives
What we offer
What we offer
  • Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investment opportunities to help you plan for the future
  • Location-specific perks and extras
  • Fulltime
Read More
Arrow Right

Sr Director, Medical Affairs

The Senior Director, UCAN Medical Affairs guides strategic and operational initi...
Location
Location
United States , Deerfield
Salary
Salary:
224000.00 - 308000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree (MD, PharmD, PhD, or equivalent scientific/clinical doctorate)
  • 10+ years of experience in Medical Affairs, Clinical, or Scientific roles within medical devices, pharmaceuticals, or combination products
  • Proven leadership of downstream and field-based medical organizations across complex portfolios
  • Deep understanding of medical governance, compliance, and scientific engagement in regulated environments
  • 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
Job Responsibility
  • Own and complete the downstream Medical Affairs strategy across Infusion Systems, IV Solutions, Clinical Nutrition, and Pharmacy products, aligned to regional and global medical objectives
  • Convert upstream medical strategy, clinical data, and evidence generation plans into tactical downstream medical plans that support launches, line extensions, lifecycle management, and in-market optimization
  • Ensure scientific and medical differentiation is clearly articulated and appropriately embedded across customer-facing medical activities
  • Lead and develop Field Medical teams (e.g., MSLs, clinical specialists) supporting downstream portfolios, ensuring consistent implementation, scientific rigor, and compliant HCP engagement
  • Coordinate Key Opinion Leader (KOL) strategy, including identification, engagement planning, and insight generation across therapy areas
  • Guide planning and execution of advisory boards, investigator meetings, educational forums, and non-promotional scientific exchanges
  • Responsible for scientific communication strategies supporting downstream portfolios, including data dissemination, congress strategy, and educational initiatives
  • Ensure accurate, balanced, and compliant communication of clinical evidence to internal and external collaborators
  • Collaborate with Medical Information, Clinical Development, and Global Medical teams to maintain uniformity in scientific narratives
  • Serve as the senior downstream medical partner to Commercial, Downstream Marketing, Sales, Training, Market Access, and Commercial Operations
What we offer
What we offer
  • Medical and dental coverage starting on day one
  • Basic life insurance
  • Accident insurance
  • Short-term disability insurance
  • Long-term disability insurance
  • Business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 401(k) Retirement Savings Plan (RSP)
  • Flexible Spending Accounts
  • Educational assistance programs
  • Fulltime
Read More
Arrow Right

Sr Director, Medical Affairs

The Senior Director, UCAN Medical Affairs guides strategic and operational initi...
Location
Location
United States , Deerfield
Salary
Salary:
224000.00 - 308000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree (MD, PharmD, PhD, or equivalent scientific/clinical doctorate)
  • 10+ years of experience in Medical Affairs, Clinical, or Scientific roles within medical devices, pharmaceuticals, or combination products
  • Proven leadership of downstream and field-based medical organizations across complex portfolios
  • Deep understanding of medical governance, compliance, and scientific engagement in regulated environments
Job Responsibility
Job Responsibility
  • Own and complete the downstream Medical Affairs strategy across Infusion Systems, IV Solutions, Clinical Nutrition, and Pharmacy products, aligned to regional and global medical objectives
  • Convert upstream medical strategy, clinical data, and evidence generation plans into tactical downstream medical plans that support launches, line extensions, lifecycle management, and in-market optimization
  • Ensure scientific and medical differentiation is clearly articulated and appropriately embedded across customer-facing medical activities
  • Lead and develop Field Medical teams (e.g., MSLs, clinical specialists) supporting downstream portfolios, ensuring consistent implementation, scientific rigor, and compliant HCP engagement
  • Coordinate Key Opinion Leader (KOL) strategy, including identification, engagement planning, and insight generation across therapy areas
  • Guide planning and execution of advisory boards, investigator meetings, educational forums, and non-promotional scientific exchanges
  • Responsible for scientific communication strategies supporting downstream portfolios, including data dissemination, congress strategy, and educational initiatives
  • Ensure accurate, balanced, and compliant communication of clinical evidence to internal and external collaborators
  • Collaborate with Medical Information, Clinical Development, and Global Medical teams to maintain uniformity in scientific narratives
  • Serve as the senior downstream medical partner to Commercial, Downstream Marketing, Sales, Training, Market Access, and Commercial Operations
What we offer
What we offer
  • Medical and dental coverage starting 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
Read More
Arrow Right

Senior Director, Corporate Affairs, CV Communications

Join Amgen's Mission of Serving Patients. At Amgen, if you feel like you're part...
Location
Location
United States , Thousand Oaks
Salary
Salary:
198606.75 - 268703.25 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree and 5 years of communications or public relations experience
  • Master's degree and 9 years of communications or public relations experience
  • Bachelor's degree and 11 years of communications or public relations experience
  • 5 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources
  • 15 or more years of experience in communications, public relations, corporate affairs, or related fields
  • Deep understanding of the biotechnology, pharmaceutical, or healthcare industry paired with significant experience in cardiovascular disease communications
  • Demonstrated ability to develop and execute integrated communications strategies tied to clear business objectives, priority audiences, insights, KPIs, and measurable outcomes
  • Strong understanding of data, analytics, social listening, media intelligence, stakeholder insights, and measurement as core inputs to modern communications strategy
  • Practical experience using AI, digital platforms, analytics, and emerging technology to improve communications strategy, execution, efficiency, measurement, and impact
  • Strong executive presence and experience counseling senior leaders on business-critical communications opportunities and challenges
Job Responsibility
Job Responsibility
  • Lead global and U.S. communications for Amgen's cardiovascular portfolio, ensuring strategies are integrated, business-relevant, and aligned across key internal partners
  • Serve as a senior communications advisor and point of accountability to global and U.S. cardiovascular leadership teams
  • Develop and execute integrated communications strategies that support business objectives, strengthen Amgen's cardiovascular story, and engage priority audiences across global and U.S. channels
  • Lead communications for marketed products, future launch readiness activities, and stakeholder-facing campaigns
  • Partner across Corporate Affairs, including Advocacy, Enterprise Media, Internal Communications, Digital and Social, Policy Communications, and other key functions, as well as Investor Relations, Medical Affairs, Legal, Regulatory, Commercial, Government Affairs, and Value & Access, to deliver integrated strategies
  • Translate scientific, clinical, and business information into clear, credible, audience-relevant communications for patients, healthcare professionals, media, advocacy partners, internal audiences, and other stakeholders
  • Successfully use data, analytics, social listening, audience insights, and measurement to inform strategy, optimize execution, and demonstrate impact
  • Identify opportunities to responsibly use AI, digital tools, and emerging technology to improve planning, content development, stakeholder engagement, workflow efficiency, and measurement
  • Inspire and manage a high-performing team by setting clear priorities, supporting development, strengthening ways of working, and maintaining high standards
  • Anticipate and navigate emerging issues, new information, stakeholder dynamics, and rapid changes in the external environment
What we offer
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
Read More
Arrow Right

Medical Science Liaison or Senior Medical Science Liaison

The Skeletal Conditions (SC) Medical Science Liaison (MSL) / Senior MSL is a reg...
Location
Location
United States
Salary
Salary:
178200.00 - 267400.00 USD / Year
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BS in life or health sciences
  • Advanced degree (MS, doctoral level) preferred
  • 3 or more years of relevant experience in clinical and 1 or more year as an MSL preferred
  • Experience in rare genetic diseases, ACH and/or Skeletal Conditions therapy preferred
  • Experience in product launch, development, and execution preferred
  • Knowledge of regulations impacting Medical Affairs and field activities in the pharmaceutical industry
  • Excellent oral and written communication, organization, and people skills
  • Proven record as a team player
  • Project management understanding and experience
  • Ability to effectively work in a virtual environment and knowledge of virtual and collaborative systems
Job Responsibility
Job Responsibility
  • Execute SC medical MSL plan and tactics within assigned territory
  • Development and periodic refinement of an approved MSL Territory Plan
  • Provide education relative to disease state and BioMarin products across product lifecycle to health care providers
  • Serve as a medical/scientific resource through answering unsolicited medical questions
  • Engage in scientific exchange and provide feedback on emerging clinical/competitive trends
  • Identify, document, discuss and communicate insights to internal stakeholders
  • Maintain clinical and technical expertise in relevant therapeutic area
  • Partner with medical and research groups and compliantly collaborate with commercial team
  • Provide support to BioMarin clinical trials including site identification and evaluation, recruitment, investigator meetings, external expert identification, and study management
  • Support clinical operations in identifying and interacting with potential investigators
What we offer
What we offer
  • Discretionary annual bonus
  • Discretionary stock-based long-term incentives
  • Paid time off
  • Company-sponsored medical, dental, vision, and life insurance plans
  • Fulltime
Read More
Arrow Right

Medical Science Liaison or Senior Medical Science Liaison

The Skeletal Conditions (SC) Medical Science Liaison (MSL) / Senior MSL is a reg...
Location
Location
United States
Salary
Salary:
178200.00 - 267400.00 USD / Year
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BS in life or health sciences
  • Advanced degree (MS, doctoral level) preferred
  • 3 or more years of relevant experience in clinical and 1 or more year as an MSL preferred
  • Experience in rare genetic diseases, ACH and/or Skeletal Conditions therapy preferred
  • Experience in product launch, development, and execution preferred
  • Knowledge of regulations impacting Medical Affairs and field activities in the pharmaceutical industry
  • Excellent oral and written communication, organization, and people skills
  • Proven record as a team player
  • Project management understanding and experience
  • Ability to effectively work in a virtual environment and knowledge of virtual and collaborative systems
Job Responsibility
Job Responsibility
  • Execute SC medical MSL plan and tactics within assigned territory to meet scientific objectives and company-defined goals for products both marketed and in development
  • Development and periodic refinement of an approved MSL Territory Plan
  • Provide education relative to disease state and BioMarin products across product lifecycle to health care providers among specialties including Genetics, Pediatric Endocrinology, Pediatric Orthopedics, and other relevant specialties
  • Serve as a medical/scientific resource through answering unsolicited medical questions and addressing other related medical information queries
  • Engage in scientific exchange and provide feedback on emerging clinical/competitive trends
  • Identify, document, discuss and communicate insights to internal stakeholders
  • Maintain clinical and technical expertise in relevant therapeutic area
  • Partner with medical and research groups and compliantly collaborate with commercial team
  • Provide support to BioMarin clinical trials including but not limited to the following: site identification and evaluation
  • recruitment
What we offer
What we offer
  • company-sponsored medical, dental, vision, and life insurance plans
  • discretionary annual bonus
  • discretionary stock-based long-term incentives
  • paid time off
  • Fulltime
Read More
Arrow Right

Senior Director, Global Real-World Evidence & Health Outcomes Research Lead, Specialty Medicines

Robust health outcomes data is necessary to support launch optimization, reimbur...
Location
Location
United States , Philadelphia
Salary
Salary:
Not provided
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD, PharmD or equivalent level qualification in health outcomes, patient reported outcomes, health economics, epidemiology, pharmacy, health, or life sciences
  • 5+ years working in global pharmaceuticals in a leadership role with line management experience
  • Strong business acumen and ability to translate customer needs into actionable data generation plan
  • Methods expertise to guide and lead team in delivering robust payer evidence deliverables and credibility to engage meaningfully with external experts & leaders in the field
  • Knowledge of the diversity and complexity of healthcare markets, health technology assessment agencies, and reimbursement decision making globally, in region and in local markets
  • Understanding of how health economics, health outcomes, comparative effectiveness research, PRO research and the use of PRO instruments can be applied at local decision-making levels, including support of clinical practice
  • Deep knowledge and strong communication skills are critical for interpreting and translating complex concepts and results effectively to a variety of audiences to impact decision making
  • Deep knowledge of drug development and therapy area
  • Strong matrix leadership and stakeholder management skills, with the ability to work independently and build credibility across the enterprise
  • Experience across product lifecycles
Job Responsibility
Job Responsibility
  • Provide leadership, management, and development of Data Generation book of work
  • Partner effectively with matrix stakeholders in planning and design of the DGP for the asset, drive disciplined execution of studies and activities, translate results, and disseminate data and research findings to all relevant internal and external stakeholders
  • Provide scientific leadership for best practice in real world evidence/ non-interventional study methodologies, including enabling external scientific advice, ensuring appropriate protocol review committee’s advice sought and incorporated
  • Drive innovation and inform ideas and options through effective engagement with external experts, clinical guideline groups, HTA agencies, methodology and policy forums, and by leveraging knowledge of the external policy and decision maker environment to enable more efficient evidence development for the asset across the lifecycle (e.g. discovery, launching and life cycle management assets)
  • Integrate excellent understanding of the evolving global health technology assessment bodies, clinical guidelines groups, policy decision makers and payer environment, including recommendation, reimbursement, pricing, and access in relevant therapy area
  • Lead discussions with key stakeholders on prioritization of data generation in order to meet business and customer needs
  • Deliver the materials to inform internal governance decision making (e.g. Medical Review Board, etc)
  • Facilitate alignment and partnership to enable more effective interactions within the complex stakeholder matrix, e.g. clinical, commercial, market access, medical affairs functions, priority market LOCs as well as external third-party suppliers
  • Represent GSK in external collaborations, engagement and scientific evidence requirements with scientific partners, reimbursement bodies and other decision makers
  • Drive quality and compliance through team to ensure trust for the evidence that is delivered
What we offer
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
Read More
Arrow Right