lead cancer therapies regulatory affairs specialist - Redwood City - beBeeLabeling

As Principal Regulatory Affairs Specialist at Pulmonx you will drive full spectrum of regulatory activities from initial market authorization through post-market compliance for our US and international device portfolio. · ...

The Clinical Affairs System Specialist II is responsible for technical systems and process related projects that support the execution of clinical trials.This role will coordinate with all members of the Clinical Affairs team and internal and external stakeholders to successfully ...

We're helping change how the world prevents, detects and guides treatment for cancer. Join our team to find a purpose-driven career. · Serve as Clinical Affairs primary contact for systems administrative tasks. · Draft system user guides and train Clinical Affairs staff on system ...

We are seeking a Clinical Affairs System Specialist II to join our team at Exact Sciences. This role will coordinate with the Clinical Affairs team and internal and external stakeholders to execute clinical trials. · ...

Job Summary: · We are seeking a highly motivated Regulatory Affairs Specialist to support the Regulatory Affairs department in ensuring compliance with the Presidio Quality Management System (QMS) and applicable regulatory bodies. In this role, you will be responsible for the tac ...

· Job Summary: · We are seeking a highly motivated Regulatory Affairs Specialist to support the Regulatory Affairs department in ensuring compliance with the Presidio Quality Management System (QMS) and applicable regulatory bodies. In this role, you will be responsible for the ...

Position Summary: · We are seeking a highly motivated Senior Regulatory Affairs Specialist to support the Regulatory Affairs department in ensuring compliance with the Presidio Quality Management System (QMS) and applicable regulatory bodies. In this role, you will be responsible ...

· Position Summary: · We are seeking a highly motivated Senior Regulatory Affairs Specialist to support the Regulatory Affairs department in ensuring compliance with the Presidio Quality Management System (QMS) and applicable regulatory bodies. In this role, you will be responsi ...

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. · ...

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 ...

We are seeking a Regulatory Affairs Specialist for a 6-month temporary contract to support regulatory activities for medical devices. · Contribute to the preparation and support of regulatory submissions and filings for U.S. FDA and other global regulatory bodies. · Assess and do ...

The Regulatory Affairs Specialist is a key partner to R&D, Quality, Manufacturing, and Marketing teams, responsible for driving regulatory strategy and ensuring compliance with global medical device regulations. · ...

The Regulatory Affairs Specialist drives regulatory strategy and ensures compliance with global medical device regulations. · ...

We are hiring for a Regulatory Affairs Specialist to work on-site at our Santa Clara location.This new team member will combine knowledge of scientific regulatory business issues to enable products including combination products that are developed manufactured or distributed to m ...

We are presently hiring for a Regulatory Affairs Specialist to work on-site at our Santa Clara CA location. Prepares robust regulatory applications to achieve departmental and organizational objectives. ...

The Regulatory Affairs Specialist is a key partner to R&D, Quality, Manufacturing, and Marketing teams, · responsible for driving regulatory strategy and ensuring compliance with global medical device regulations. · Develop regulatory strategies for new product introductions and ...

The Regulatory Affairs Specialist supports and executes regulatory activities for medical devices across the product lifecycle, with increasing independence and responsibility. This role contributes to regulatory strategy, prepares and manages submissions and registrations, condu ...

+ Work that matters · Grow and learn · Care for yourself and your family · Be your true self+Career development with an international company where you can grow the career you dream of. · Excellent retirement savings plan with high employer contribution. · Tuition reimbursement · ...

· Who We Are · RefleXion is a privately held theranostic oncology company located in Hayward, CA, commercializing SCINTIX biology-guided radiotherapy, a novel therapy that uses a single radiotracer injection to turn cancer cells into real-time biological beacons to guide extern ...

+ Job Overview · Under general supervision, Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients. · +Bachelor's Degree in Lifescience or related discipline. · At least ...

We're transforming how regulatory documents get written in pharma biotech and medtech through fundamental AI research. · The Role · You'll be teaching AI systems how to think like a regulatory professional evaluating AI-generated content identifying gaps in logic or compliance de ...