Associate Director, Clinical Affairs - Irvine, CA

The Manager Clinical Affairs will be responsible for case planning for global clinical trials and collaborating with internal and external stakeholders on CRB process development, execution, and improvement. · ...

Reporting to the Director of Clinical Affairs, the Manager, Clinical Affairs (CRB) will be responsible for case planning for global clinical trials and collaborating with internal and external stakeholders on CRB process development, execution, and improvement. · This position pr ...

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 ...

We are looking for a highly motivated Medical Affairs Clinical Specialist to serve as the clinical medical and scientific lead for clinical trials in the J&J MedTech Neurovascular portfolio. · ...

· We are the makers of possible · BD is one of the largest global medical technology companies in the world. · ...

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

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 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 ...

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 ...

We believe that the human element, across our global teams, is what allows us to continually evolve.As part of BD's Advanced Patient Monitoring (APM) portfolio, the Manager,Clinical Affairs is responsible for leading and managing clinical research activities that support product ...

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 ...

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 ma ...

+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 Post-Market Regulatory Affairs Specialist represents the Regulatory Affairs function and is responsible for knowledge of requirements and processes for maintaining a product in the clinical setting. · A strong candidate must have Medical Device IDE (clinical trial) experience ...

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 ...