Global Regulatory Affairs Executive - Santa Clara - beBeeRegulatoryAffairs

Gilead es una empresa biotecnológica que busca crear un mundo más saludable para todos. Estamos buscando a personas apasionadas y ambiciosas que estén dispuestas a hacer una diferencia directa. · Desarrollar e implementar planes de acción para USMA Viral Hepatitis, PBC y COVID-19 ...

The Executive Director, Medical Affairs, Lung is a key leader and subject matter expert responsible for shaping and executing the medical affairs strategy in lung cancer. · ...

The Executive Director Medical Affairs GI is a key leader and subject matter expert responsible for shaping and executing the medical affairs strategy in GI cancers. This role oversees the development and implementation of medical affairs plans for lung-related indications includ ...

The Executive Director of Medical Affairs for Lung is a key leader and expert in lung cancer responsible for shaping and executing the medical affairs strategy. · ...

The Executive Director, Medical Affairs, GI is a key leader and a subject matter expert responsible for shaping and executing the medical affairs strategy in GI cancers. · Strategic Leadership Develop and lead the US medical affairs strategy for GI cancers. · Foster a culture of ...

+ Summarize the job description: Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life and resolving serious unmet medical needs. · The Executive Director will collaborate within ...

The Executive Director will lead medical affairs strategy in lung cancer. The role oversees launch excellence for multiple indications lifecycle management and scientific engagement. · Advanced scientific degree required. · Minimum of 12+ years progressive Medical Affairs or rela ...

A great place to work.Careers At Summit Therapeutics Sub, Inc.Current job opportunities are posted here as they become available.Executive Director, Global Medical Affairs, LungJob Summary: · The Executive Director Medical Affairs will be responsible for shaping and executing the ...

The Executive Director Global Medical Affairs GI oversees medical affairs plans for lung-related indications including launch excellence lifecycle management scientific engagement. Recent hands-on experience in GI cancers either clinical practice pharmaceutical companies required ...

We are looking for bright and talented individuals to join our team and share in our passion and commitment to improving the lives of patients. · Provide leadership of the strategy and development of Lirentelimab's annual Medical Plans and ensure hands-on implementation of key ac ...

The Regulatory Affairs Specialist supports global regulatory strategy and execution for medical device products ensuring compliance with FDA and international regulations throughout the product lifecycle. · ...

This role provides compliance and quality system support to the Regulatory Affairs organization. · Drive preparation and maintenance of key performance indicator dashboards · Support audit preparedness initiatives through risk identification, mitigation planning, and preventive a ...

We're looking for a proactive and organized Personal Assistant to join our team If you're fluent in Mandarin and English, ...

This role will provide compliance support to the Regulatory Affairs organization by driving preparation of KPI dashboards and maintaining a pulse on formal RA management review and internal metricsSupporting quality system integration for acquisitions and new product introduction ...

The Regulatory Affairs Manager is responsible for monitoring regulatory requirements that impact HVAC products within the West Coast region. · ...

The Senior Regulatory Affairs Specialist is responsible for managing and executing regulatory activities for Class III implantable medical devices that require governmental approval. · Prepare, author, and submit PMA supplements · ...

The Regulatory Affairs Specialist supports global regulatory strategy and execution for medical device products ensuring compliance with FDA and international regulations throughout the product lifecycle. · This role partners closely with R&D Quality Manufacturing and Clinical te ...

This role provides compliance and quality system support to the Regulatory Affairs organization. · ...

We are looking for a proactive and organized Personal Assistant to join our team. · ...

We operate with a purpose-driven, agile, and collaborative culture, where every team member contributes to advancing solutions that improve patient outcomes. · As the Director of Clinical Affairs at VahatiCor, you will be at the forefront of driving and managing the execution of ...

This position works out of our Santa Clara, CA location in the Vascular division. · Facilitates development of clinical strategy and trial design by interacting with study PIs, · Research & Development, Regulatory Affairs, · & Biostatistics. · ...