Associate Director, Clinical Affairs - Irvine

We are looking for a highly motivated Medical Affairs Clinical Specialist to be part of our Medical Affairs team in Johnson & Johnson MedTech - Neurovascular. · This role provides medical oversight, clinical direction and scientific expertise throughout study design, execution an ...

At Johnson & Johnson,?we believe health is everything. Our strength in healthcare innovation empowers us to build a?world where complex diseases are prevented, treated, and cured,?where treatments are smarter and less invasive, and?solutions are personal.?Through our expertise in ...

Johnson & Johnson is recruiting for a Medical Affairs Clinical Specialist located in Irvine, California. · We are looking for a highly motivated Medical Affairs Clinical Specialist to be part of our Medical Affairs team in Johnson & Johnson MedTech – Neurovascular.This role provi ...

+We are the makers of possible BD is one of the largest global medical technology companies in the world Advancing the world of health is our Purpose and it's no small feat It takes the imagination and passion of all of us from design and engineering to the manufacturing and mark ...

+We are looking for a highly motivated Medical Affairs Clinical Specialist to be part of our Medical Affairs team in Johnson & Johnson MedTech - Neurovascular. · ++Serve as the primary study medical lead for company sponsored clinical studies. · +Support the clinical trial team t ...

We are looking for a highly motivated Medical Affairs Clinical Specialist to be part of our Medical Affairs team in Johnson & Johnson MedTech – Neurovascular. · ...

This is an exciting opportunity to join a growing company that focuses on precise, early detection of emerging diseases. The Director of Clinical Affairs is responsible for the day-to-day planning and execution of clinical and regulatory activities across the diagnostic portfolio ...

This is an exciting opportunity to join a growing company that focuses on precise, · early detection of emerging diseases.The Director of Clinical Affairs is responsible for the day-to-day planning and execution · of clinical and regulatory activities across the diagnostic portfo ...

+Job Summary · We are seeking a Senior Manager Clinical Affairs to lead strategic initiatives within our Advanced Patient Monitoring portfolio. · +ResponsibilitiesManage clinical operations team. · Oversight of high-performing clinical operations teams. · Liaise with R&D Regulato ...

The Director of Clinical and Regulatory Affairs owns the clinical and regulatory strategy for Pangea's diagnostic portfolio, including prioritization, sequencing, and execution of clinical programs and regulatory submissions. · ...

+Job summary · Pangea Laboratory is seeking a Director of Clinical and Regulatory Affairs to lead the clinical and regulatory strategy for its diagnostic portfolio. · +ResponsibilitiesDefine and own the clinical strategy for Bladder CARE and future diagnostic programs. · Contribu ...

This recruitment is for Temporary Regulatory Affairs Coordinator position through UCI's internal temporary staffing service. · Duties include but are not limited to: Ensure successful management of the regulatory aspects of each study conducted through UCI's Center for Clinical R ...

The Temporary Clinical Regulatory Affairs Coordinator will ensure successful management of the regulatory aspects of each study conducted through UCI's Center for Clinical Research. · Ensure successful management of the regulatory aspects of each study conducted through UCI's Cen ...

Chapman University School of Pharmacy (CUSP), in collaboration with Amgen Inc., offers a fellowship in Oncology Medical Affairs. · Shadow inter-professional team at clinical sites. · Maintain compliance with policies and procedures. · Provide drug information responses under clos ...

The Senior Vice President, Medical Affairs serves as the enterprise clinical and scientific leader responsible for shaping and executing Masimo's global medical affairs strategy. · This role provides executive oversight of clinical engagement, evidence generation, scientific comm ...

The Medical Affairs Analyst will be a key member of the Office of the Chief Medical Officer (CMO) and serve an important role in building MicroPort's unified medical and evidence infrastructure. · This is an ideal role for a scientifically trained, detail oriented, and articulate ...

We are seeking a Senior Manager of Regulatory Affairs to lead regulatory strategy and execution for Class III cardiovascular medical devices. The ideal candidate has deep experience with PMA submissions, EU MDR requirements, and post-market activities within high-risk implantable ...

· We are searching for a Director of Regulatory Affairs with deep expertise in invasive electromechanical medical devices and extensive experience preparing and submitting 510(k) notifications. · Leads the preparation, submission, and negotiation of 510(k) premarket notification ...

Responsible for timely preparation and submission of organized, scientifically valid global regulatory affairs submissions (clinical, pre-, and post-market applications), query responses and correspondence tracking. Maintains regulatory information for competitive intelligence, l ...

We are looking for a highly motivated and knowledgeable Associate Director - Medical Science Liaison (MSL) who specializes in cardiovascular medicine, · Support the development and implementation of strategic engagement plans to establish and maintain relationships with KOLs, · A ...