Global Medical Affairs jobs

Now available 96 results are consistent

Sort by:relevance - date

DIRECTOR, GLOBAL MEDICAL AFFAIRS STRATEGY AND EXECUTION, SPECIALTY OPHTHALMOLOGY

GMAF Strategic Plans co-development of a consolidated global Medical Affairs Strategy (MAS) that meets prioritized global and regional strategic imperatives; providing expert knowledge in the MAS planning process; driving the c...

CompanyJohnson & Johnson
AddressRaritan, NJ
CategoryHealthcare
Date Posted 3 hours ago See detail

Director, Global Medical Affairs Strategy and Execution, Specialty Ophthalmology New

Johnson & Johnson

Raritan, NJ

GMAF Strategic Plans co-development of a consolidated global Medical Affairs Strategy (MAS) that meets prioritized global and regional strategic imperatives; providing expert knowledge in the MAS planning process; driving the c...

Global Medical Affairs Lead, Uplizna

Amgen

Washington, DC

Serve as the Medical Affairs Representative on various global strategic teams.. Support the development of the integrated evidence generation plan for neuromyelitis optica spectrum disorder and other follow-on indications.. Captur...

Global Medical Affairs Lead, Uplizna

Biospace

Washington, DC

Serve as the Medical Affairs Representative on various global strategic teams. Support the development of the integrated evidence generation plan for neuromyelitis optica spectrum disorder and other follow-on indications. Capture...

Senior Director, Head of Global Medical Affairs for Pulmonary Hypertension

Johnson & Johnson

Raritan, NJ

Provide medical leadership in interactions with external stakeholders (HA bodies, external experts, advisory boards). Execution: Provide leadership, scientific input and guide the development of key Medical Affairs deliverables...

Director, Global Medical Affairs Lead

Biospace

Waltham, MA

Serve as a medical subject matter expert on ASOs and other therapeutic modalities for our NMD programs. Serve as internal expert on medical literature / data associated with our NMD programs. Represent GMA on cross-functional team...

Senior Medical Scientist - Global Medical Affairs Oncology Solid Tumor Early Products New

Biospace

Washington, DC

Contribute to the Global Medical strategy through deep understanding of medical practice Provide support for the development and achievement of the clinical development plan for the oncology products through strategic medical insi...

Global Senior Director Medical Affairs (GDMA) – Daiichi Alliance, Oncology

Merck Sharp & Dohme

Rahway, NJ

$200,200 - $315,100 a year

The Global Senior Director Medical Affairs (GDMA) is responsible for driving execution of scientific & Medical Affairs plans for their assigned Therapy Areas (TA) in key countries and regions. They are impactful members of Product...

Global Medical Affairs Leader, Gastroenterology

Johnson & Johnson

United, PA

Development of Medical Affairs Strategy and plan for the assigned compounds based on global and prioritized regional needs. Working with the CDT to ensure integration with the overall global compound strategy, resulting in one g...

Senior Director– Global Medical Affairs, Lilly Diabetes and Obesity

Biospace

Remote - Indiana, United States

Specific activities include developing or contributing to the global and/or regional clinical/medical plan in his/her therapeutic area of responsibility, the development, conduct and reporting of local clinical trials; the implem...

Associate Director, Congress Strategy Lead, Global Medical Affairs Oncology

Biospace

Boston, MA

Co-develop Oncology external engagement strategy and lead the development of the cross-portfolio Congress Strategy and narrative for global congresses.. Liaise cross-functionally within Global Medical Affairs Oncology, and with OT...

Senior Director, Global Medical Affairs Strategy - Solid Tumors

Genmab A/S

Princeton, NJ

Develop and execute the overall Medical Affairs Strategy for designated product in NSCLC therapeutic area. Serve on Compound Development Team as Global Medical Affairs representative; Co-Lead Global Commercialization Team. Serve a...

Associate Director, Global Medical Affairs Phase 4 Research in HIV Treatment

Biospace

California, United States

Lead and support GMA-led Phase 4 Research studies in HIV Treatment, specifically for B/F/TAF data generation priorities related to the IRA submission, and as articulated through Gilead strategy documents [BVY indication strategic...

Global Medical Affairs Leader Actions

Johnson & Johnson

Raritan, NJ

Minimum of a relevant masters or doctorate level advanced scientific/medical degree (e.g. MD, PhD, PharmD), with experience in oncology required with a strong preference for lung and head & neck cancer experience.. Prior experie...

Director, Global Medical Affairs - Oncology

Biospace

Cambridge, MA

Provide subject matter area expertise and leadership for cross-functional internal workstreams including Pharmacovigilance, Biostatistics, Clinical Operations, Regulatory Affairs and Brand teams.. Develop and foster relationships...

Medical Director, Global Medical Affairs - Inflammation/Allergy

Biospace

Washington, DC

Assisting the US Medical-Asset Leader in the execution of US product medical strategy, via implementation of the US Medical Plan. Activities include developing tactics aligned with the US strategy and supporting indications via su...

Medical Affairs-Scientific Director CV Renal

Biospace

Plainsboro, NJ

Identify and anticipate potential trends, changes to market conditions and areas of opportunity aligned with Therapeutic Area priorities. Utilizes subject matter expertise and analytical tools to provide deeper customer knowledge...

Medical Director, Bladder - Global Medical Affairs Oncology

Johnson & Johnson

Raritan, NJ

This position requires a minimum of an advanced degree in medicine (i.e. M.D. or equivalent). A trained Oncologist, or an individual with substantial previous experience in conducting oncology clinical studies is highly desired....

Medical Director, Global Medical Affairs (Neurology)

Ultragenyx Pharmaceutical

Remote - Oregon, United States

Develop and lead the neurology therapeutic medical strategy for the assigned therapeutic programs.. Develop and lead the integrated evidence generating plan for the neurology therapeutic programs.. Lead execution of the relevant...

Clinical Trial Manager, Global Oncology Medical Affairs

Biospace

Basking Ridge, NJ

Support the preparation, set-up, and execution and reporting of all Global Oncology Medical Affairs operations Clinical Trial activities, ensuring adherence to timelines, budgets, project, and quality plans, and relevant ICH/GCP G...

Manager, Global Regulatory Affairs, Marketed Products - Now Hiring

Takeda Pharmaceutical

Bronx, NY

$186,000 per year

By clicking the Apply button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas and. I further attest that...

VP/TA Head, General Medicine - Global Regulatory Affairs

Merck

Rahway, NJ

Developing an active engagement strategy with US FDA and global health authorities to advocate advanced regulatory strategies for novel medicines.. Contributing to the continuous improvement of the operating model for regulatory a...

Manager, Global Regulatory Affairs CMC - Now Hiring

Takeda Pharmaceutical

Brooklyn, NY

$133,200.00 to $223,200.00 per year

I further attest that all information I submit in my employment application is true to the best of my knowledge.Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC in Cambridge, MA with the...

Functional Learning Partner, Commercial and Medical Affairs

Biospace

Cambridge, MA

Learning and Upskilling Strategy: Work with business leaders and HR business partners in the functions you support to develop an actionable learning and upskilling strategy focused on priority skills and performance outcomes. Serv...

Assoc. Director, Field Medical Affairs-Hematology (northern CA)

Biospace

United States

Territory: Northern CA, NevadaA typical day may include the following: Identifying and maintaining a list of relevant medical/therapeutic area experts, investigator targets and associated plans of action.Establishing, fostering, c...

Vice President/ Senior Vice President, Medical Affairs

Biospace

South San Francisco, CA

As a key member of the leadership team, provide deep medical and scientific expertise on Medical Affairs, launch, and lifecycle strategies. Lead the full spectrum of the Medical Affairs functions that are responsible for the devel...

Senior Director/Director, Global Regulatory Affairs Early Respiratory & Immunology

Astrazeneca

Boston, MA

Work on cross-project initiatives of high importance for the early R&I portfolio. Lead the development and implementation of innovative global strategies of increasing complexity to improve the likelihood of regulatory success. Ac...

Specialist, Medical Affairs

Becton Dickinson

Franklin Lakes, NJ

Works with manager to understand full needs of Medical Affairs (MA) function as it relates to Post Market Surveillance (PMS) Program and annual Post Market Surveillance activities (PMS Plan and Periodic Safety Update Report, PSUR)...

Manager, Global Regulatory Affairs CMC Submissions Management - Now Hiring

Takeda Pharmaceutical

New York, United States

$138,500 - $186,000 per year

I further attest that all information I submit in my employment application is true to the best of my knowledge.Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC Submissions Management in...

OOS Case Manager (US Medical Affairs CAR-T)

Johnson & Johnson

United, PA

Coordinate, supervise and manage all aspects of commercial out-of-specification products life cycle. Lead and partner with multiple internal functions including MSLs, Supply Chain, Safety Management, Quality Assurance, Medical Af...

Senior Manager/Associate Director, Regulatory Affairs, Strategic Global Labeling - Combination

Biospace

North Chicago, IL

Develop and direct strategic regulatory planning, creation, and revision of labeling for combination product and device submissions (pre and post approval) with an understanding of Global requirements to lead the Labeling Sub team...