Global Medical Lead Job at Dompé (San Mateo)

Vp, Global Medical Lead Respiratory (tslp)

The VP, Global Medical Lead (GML) Respiratory (TSLP) is a key senior business le...

Location

United Kingdom; United States , London; Collegeville; Upper Providence

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Medical Doctor, Pharmacist or PhD
Therapy Area experience/expertise in Respiratory
In country experience as a Therapy Area Medical Lead or Country Medical Director
Experience directing the strategy of an asset at a global level
Experience working in clinical development
Expertise in launching an asset at local and global level
Asset lifecycle management expertise at local and global level
Expertise in Data Generation in terms of asset development
Experience of omnichannel strategies

Job Responsibility

Lead both the cross-functional product medical team (PMT) and product development at the Global level
As convenor and chair of the PMT
Jointly accountable for developing the global medical brand strategy and plans for TSLP
Set direction along strategic framework of the medical brand plan including setting scientific objectives, owning the medical scientific narrative and the integrated communication plan
Accountable for directing and coordinating global resources to generate data and create content to support priority markets, leveraging the expertise of the Global operations team and Global data team
Represent medical in cross-functional strategy meetings and workshops, and proactively offer options for innovative medical strategy for the Integrated Asset Plan (IAP) at the Product Development Team (PDT) and Product Commercial Team (PCT) meetings
Provide focused support at key inflection points during development (e.g., launch)
As Lead of PMT and medical product team at Global level
Responsible for representing the voice of the Chief Patient Officer (CPO) Organization for TSLP
Accountable for all medical activities related to product development at the global level

Fulltime

Vice president, global obesity medical lead

The Vice President, Global Obesity Medical Lead will report to the Head of Medic...

Location

United States , New York City; Cambridge

Salary:

300100.00 - 467400.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

MD, PharmD, or PhD required
More than 10 years with PharmD/PHD or more than 9 years with MD in the medical affairs function in the pharmaceutical industry
In-depth Obesity experience strongly preferred
Experience with patient care, especially in specific therapeutic area preferred
Deep understanding of HCP informational needs
Scientific translational research background and ability to understand, interpret, and communicate scientific literature
In-depth understanding and experience with study methodology, protocol design, safety evaluation, and data analysis
Proactive, pragmatic, flexible person with excellent leadership qualities, strategic thinking, communication & presentation skills
An ability to lead and manage in a matrixed structure and in a collaborative team environment
Extensive knowledge of patterns of medical practice and healthcare delivery and current and evolving landscape

Job Responsibility

Partner cross-functionally to develop integrated plans for supporting the pipeline and inline Pfizer Obesity portfolio
Provide exceptional oversight of environmental, disease state, competitor, asset analysis
Ensure the development of rapid data analytic capacities
Develop novel data generation strategies
Provide portfolio oversight
Develop standardized strategic tools and metrics
Ensure substantial medical input into all Asset Medicines Plans
Engage on peer basis with medical directors of independent networks and other healthcare providing entities
Chairs or leads the Global Medical Affairs Team
Represents medical affairs globally at the relevant asset team and/or other appropriate teams and committees

What we offer

Eligibility for participation in Pfizer’s Global Performance Plan with a bonus target of 30.0% of the base salary
Eligibility to participate in our share based long term incentive program
401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
Paid vacation, holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage
Relocation assistance may be available

Fulltime

Global Scientific & Medical Publications Lead, Vaccines

Global Scientific & Medical Publications Lead, Vaccines at Sanofi. The role invo...

Location

United States , Morristown

Salary:

178500.00 - 257833.33 USD / Year

Sanofi

Expiration Date

Until further notice

Requirements

Prior relevant experience in scientific and medical publications management
Up-to-date knowledge of current publication-related regulations, recommendations, best practice, technologies, formats, and guidelines
Significant experience in the pharmaceutical industry, preferably in medical affairs (global, regional, or local)
Proven experience of building strong working relationships internally and externally to achieve results
Demonstrated ability to collaborate and share information to contribute to the medical planning process and execute the agreed plan in line with objectives
Demonstrated ability as a proactive and effective team player
Experience working within large multinational teams with a high performing culture
Bachelor's degree in Life Sciences, Public Health, or related field
Minimum of 5 years of experience in the pharmaceutical industry, with at least 3 years of medical publications experience
Strong working knowledge of ICMJE and good publication practice industry guidelines

Job Responsibility

Manage appropriate and balanced assignment of projects across the members of the Scientific & Medical Publications team
Manage publications planning and operational activities for a selected franchise/product
Expand company-wide communication, visibility, and training around publications
Ensure Publication Managers are involved in all company publication activities
Provide a single, company-wide vision of Sanofi Vaccines' publication activities
Ensure company-wide compliance with Sanofi policy and Good Publication Practices
Manage direct resources and effectively collaborate with Sanofi Global BO/Hub to support Sanofi Vaccines' publication activities
Act as representative of Vaccine Medical in X-GBU scientific and publications community
Act as representative of Vaccine Medical within the Sanofi iEnvision team and with CMO organization
Act as representative of Vaccine Medical Publications in implementation of iEnvision and other tools, systems and processes

What we offer

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

Fulltime

Medical Director, Global Evidence Generation Lead

The medical Director, evidence generation is responsible for supporting strategi...

Location

Belgium , Mechelen

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

Requirements

Minimum of 7+ years of experience in evidence generation, clinical development, HEOR, or a related field
At least 5 years of experience in Epidemiology, Health Economics Outcomes Research (HEOR), or/and Health Systems Research
Proven track record of developing and implementing integrated evidence generation plans in the pharmaceutical or biotechnology industry
Experience in design, conduct and oversight of real-world evidence studies ranging from protocol writing to project management oversight and data interpretation and communication
Solid understanding of the cross functional drug development lifecycle and processes (Business Development, clinical trial design, conduct, & endpoint selection, Clinical Operations, Data Management, Biostatistics, and Regulatory)
Demonstrated expertise and experience working with methods for evidence generation using primary and secondary data sources, knowledge of common issues and challenges of implementation, and track-record of successful publications
Demonstrated depth of understanding of observational research methods, regulatory standards, and ability to leverage epidemiologic and data science expertise to meet evolving business needs
Evidence of technical expertise of applying pharmacoepidemiology evidence and insights at the therapy/product level
Ability to explain strengths and limitations of clinical practice datasets — such as electronic health records, claims, clinical data registries, patient generated health data, and other health data sources — in context of designing pharmacoepidemiology study designs
Ability to work successfully in a matrix and quick paced environment

Job Responsibility

Collaborate with cross-functional colleagues to Lead the development and execution of Medical evidence generation strategy and tactics supporting products in development as well as those commercially available, with appropriate prioritization and use of resources ensuring alignment with corporate goals, regional needs, and therapeutic priorities
Oversee the Design and implementation of Integrated Evidence Generation Plans (IEGPs) that incorporate clinical, real-world, and economic data to support product positioning and value demonstration
Scope RWE studies (Regional/National/Academic/Patient/Vendor), selection of new or existing academic (can include: ISR/lIS/NIS)/non-governmental registries (retrospective/prospective), management across various phases from start up, maintenance to final deliverables
Translate (early) trial efficacy to real-world comparative effectiveness as part of early and late phase study planning, identification of subpopulations, and for potential risk-sharing purposes
Design and implement multiple database and/or de novo (e.g. registries) pharmacoepidemiologic studies, as well as literature reviews, intended to provide insight into background epidemiology, disease state regular care, and/or quantify benefits and/or risks potentially associated with Alfasigma products
Project management oversight – ensuring effective design, initiation and implementation of real world evidence studies, while ensuring effective study protocols and plans, managing budget and milestone tracking, and where appropriate contracting with partner organizations
keep abreast on new data and developments in the field, key publications of interest, research methodologies and regulatory standards across the EU and New Markets regions and proactively address HOR strategy changes in collaboration with global and regional teams in anticipation of any trends
Review and provide relevant RWE/HOR inputs to statistical analysis plans and analysis outputs
Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team
Establish metrics to evaluate the effectiveness and impact of evidence generation activities on corporate and product-specific objectives

What we offer

We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development

Associate Director, Global Medical Publications

The Associate Director of Publications leads the strategic development in close ...

Location

United States

Salary:

Not provided

The Muse

Expiration Date

Until further notice

Requirements

Degree in nursing, pharmacy, or advanced degree in science/medicine (MD, PhD, Pharm D, MS) preferred with 10+ years of pharmaceutical/biotherapeutics industry or relevant experience
Scientific and medical communication excellence
Strategic thinking with strong execution capability
Cross-functional collaboration and stakeholder management
Compliance mindset and attention to detail
Ability to manage complexity and multiple priorities
Continuous improvement and innovation orientation

Job Responsibility

Partners with cross-functional teams to develop the pub plan for a DA
Responsible for tracking timely documentation of all publications for assigned DA
Leads operational execution of all publication activities within a DA
Leads training activities of publication systems and processes
Partner closely with team members, Compliance, and cross-functional stakeholders to establish and uphold ethical, transparent, and responsible publication practices
Responsible for the audits of pubs with escalation to the Director as appropriate for assigned DA
Collaborate enterprise-wide to harmonize processes, SOPs, trackers, and governance frameworks ensuring compliance with internal and external regulations
Drive publication metrics, including altmetrics, share-of-voice dashboards, and usage/citation tracking, to measure and communicate scientific impact
Innovate in data dissemination through digital channels, advanced analytics, and enhanced reporting capabilities for assigned DA
Responsible for independently representing Global pubs at strategic meetings for assigned DA

What we offer

Health Insurance
Dental Insurance
Vision Insurance
Life Insurance
Short-Term Disability
Long-Term Disability
FSA
HSA
Mental Health Benefits
Adoption Leave

Fulltime

Senior Director, Global Medical Affairs, Oncology

Moderna is seeking a Global Medical Director to lead medical affairs strategy ac...

Location

United States , Cambridge

Salary:

210900.00 - 379200.00 USD / Year

Moderna

Expiration Date

July 13, 2026

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

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

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

Senior Director, Global Medical Affairs – Front Line Care

Senior Director, Global Medical Affairs – Front Line Care (FLC) is the senior me...

Location

United States , Skaneateles Falls

Salary:

280000.00 - 385000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

8-10+ years of industry experience, including meaningful experience in MedTech
5+ years of strategic leadership/management experience, including people leadership in a matrixed environment
Demonstrated experience developing and implementing global evidence roadmaps
Leading/partnering on clinical evidence strategy, scientific communications, and cross-functional decision-making
Strong understanding of the U.S. and Global regulatory and healthcare environment including EuMDR and notified bodies requirements
Proven track record to operate with high integrity and in alignment with compliance standards
Demonstrate solid proficiency in study build, clinical trial methodology
Applicants must be authorized to work for any employer in the U.S.

Job Responsibility

Define and implement the FLC Global Medical Affairs strategic plan and critical evidence priorities
Provide senior medical leadership and decision support for business strategy, innovation, and new product development
Translate clinical, scientific, and customer insights into clear strategic recommendations and measurable execution plans
Develop global clinical evidence roadmap enabling execution of the global business priorities
Serve as a senior representative for FLC with KOLs, professional societies, advisory boards, and scientific conferences
Build strong, trusted partnerships across R&D, Regulatory Affairs (RA), Quality, Marketing, Reimbursement, Regions, Market Access, and Patient Safety
Partner with Global Patient Safety as a product/therapy to provide subject matter expert support
Provide expert medical/scientific leadership for due diligence on business development opportunities
Lead, coach, and develop a high-performing Medical Affairs team.

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
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

Senior Director, Global Medical Affairs – Front Line Care

Senior Director, Global Medical Affairs – Front Line Care (FLC) is the senior me...

Location

United States , Skaneateles Falls

Salary:

280000.00 - 385000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

8-10+ years of industry experience, including meaningful experience in MedTech
5+ years of strategic leadership/management experience, including people leadership in a matrixed environment
Demonstrated experience developing and implementing global evidence roadmaps
Leading/partnering on clinical evidence strategy, scientific communications, and cross-functional decision-making
Strong understanding of the U.S. and Global regulatory and healthcare environment including EuMDR and notified bodies requirements
Proven track record to operate with high integrity and in alignment with compliance standards
Demonstrate solid proficiency in study build, clinical trial methodology
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

Define and implement the FLC Global Medical Affairs strategic plan and critical evidence priorities
Provide senior medical leadership and decision support for business strategy, innovation, and new product development
Translate clinical, scientific, and customer insights into clear strategic recommendations and measurable execution plans
Ensure strong expertise in study build, clinical trial methodology, and evidence-generation guidelines
Develop global clinical evidence roadmap enabling execution of the global business priorities
Lead the evidence-generation strategy across the product lifecycle
Accountable for Baxter-sponsored clinical research for FLC, ensuring scientific integrity and compliance with Good Clinical Practice (GCP)
Create appropriate partnerships internally and externally to develop health economics & outcomes research (HEOR) needs
Develop and lead 3rd party relationships (e.g. CROs) as required to implement study deliverables
Serve as a senior representative for FLC with KOLs, professional societies, advisory boards, and scientific conferences

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

Select Country

Global Medical Lead

Job Description

Job Responsibility

Requirements

What we offer

Looking for more opportunities?