Sr. Manager, GCP Compliance - San Diego - Xencor

The Associate Director leads quality assurance activities to protect data integrity and regulatory readiness across Acadia Pharmaceuticals' nonclinical and clinical portfolio. ...

+Job summary: · About Acadia Pharmaceuticals · Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world.+ · +Plan schedule coordinate conduct internal external ...

The Associate Director plays a critical role in protecting data integrity and regulatory readiness across the company's nonclinical and clinical portfolio. · Plan, schedule, coordinate, and conduct internal and external GLP/GCP audits of company functions and Contract Service Pro ...

A GCP Specialist will support GCP compliance for clinical operations to ensure regulatory adherence. They will assist in compliance processes and collaborate with cross functional teams to maintain clinical trial integrity. · Develop, implement, and maintain systems to ensure GCP ...

About the Role: · Responsible for driving and leading Clinical Quality Assurance (CQA) activities in support of research projects across multiple therapeutic areas for development and commercial products. Provides Quality Assurance ("QA") expertise, leadership and training to ens ...

Clinical Quality Assurance – GCP Specialist will support GCP compliance for clinical operations to ensure regulatory adherence. · ...

As a GCP Specialist at Capricor Therapeutics, you will support GCP compliance for clinical operations to ensure regulatory adherence. You will assist in compliance processes and collaborate with cross-functional teams to maintain clinical trial integrity. · ...

About Artiva: · Artiva is clinical-stage, publicly-traded biotechnology company focused on developing natural killer (NK) cell-based therapies for patients suffering from devastating autoimmune diseases and cancers. Artiva's lead program, AlloNK, is an allogeneic, off-the-shelf, ...

Support GCP compliance for clinical operations to ensure regulatory adherence. · ...

· Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne m ...

About the Role: · Responsible for driving and leading Clinical Quality Assurance (CQA) activities in support of research projects across multiple therapeutic areas for development and commercial products. Provides Quality Assurance ("QA") expertise, leadership and training to ens ...

We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. · Serve as the CQA Lead for complex programs. · Develop risk mitigation plans and strategies. · ...

Who We Are: · At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering ...

We are looking for an Executive Director of Clinical QA who will provide vision, strategic planning and management for departmental initiatives. The role includes developing and setting strategy and operating plans for Clinical QA, establishing compliance procedures and quality l ...

Arrowhead Pharmaceuticals, Inc. (Nasdaq:  ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead ther ...

Arrowhead Pharmaceuticals, Inc. (Nasdaq{{:}} ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead t ...

Key Responsibilities: · Act as Principal or Sub-Investigator for clinical trials in Dermatology and Endocrinology. · Conduct thorough medical evaluations to determine patient eligibility for studies. · Maintain vigilant monitoring of adverse events to ensure participant safety at ...

Clinical Research Coordinator Independently manage assigned studies at the Mission Valley site with Research Assistant support. · ...

Responsible for driving and leading Clinical Quality Assurance (CQA) activities in support of research projects across multiple therapeutic areas for development and commercial products. · Provides Quality Assurance ("QA") expertise, leadership and training to ensure adherence wi ...

body{font-family:Arial;}p{margin-bottom:15px;}Pain Management Physician · Clinical trial physician sought to lead innovative studies in pain management. Ideal candidate is a board-certified medical professional with expertise in overseeing participant care, ensuring protocol comp ...

A clinical research site manager oversees the day-to-day operations of a clinical trial site to ensure studies are conducted safely ethically and in compliance with regulations. · Manage all aspects of clinical studies at the site ensuring adherence to protocols ethical guideline ...