GCP Specialist - San Diego

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. · ...

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

As a GCP Specialist you will support GCP compliance for clinical operations to ensure regulatory adherence. · Develop implement and maintain systems to ensure GCP compliance. · Provide GCP support to clinical study teams to reduce compliance risks. · Collaborate with Quality Assu ...

We are seeking an experienced TMF Specialist to manage paper and electronic Trial Master Files across clinical studies. · Bachelor's degree in Life Sciences or advanced degree. · 4+ years' experience managing eTMF systems, including Veeva Vault. · ...

We are seeking an experienced TMF Specialist to manage paper and electronic Trial Master Files across clinical studies. This role supports TMF operations, ensuring quality, timeliness and compliance in collaboration with internal teams CROs and TMF vendors. · ...

The Clinical Trials Manager provides operational leadership of assigned clinical trials. · Project Management · Financial Tracking · ...

The individual in this position is responsible for performing day-to-day quality assurance (QA) activities, · Maintain, troubleshoot, and monitor the effectiveness of the POCRL's Quality Management System (QMS) · Ensure that POCRL activities conform with the requirements of the l ...

The Clinical Trials Manager provides operational leadership of assigned clinical trials to ensure delivery on time, within budget, and of high quality in compliance with ICH GCPs, regulations/guidelines. · Project ManagementFinancial Tracking · ...

This position is responsible for the regulatory lifecycle management of oncology clinical trials.The specialist serves as the primary liaison between Principal Investigators, institutional review boards (IRBs), federal agencies (FDA), and industry sponsors to ensure all research ...

The Clinical Supply Chain Manager will support activities related to Clinical Trial Material (Phase 1-4) and provide operational support services to the CMC Development and Commercial Supply Chain/Manufacturing functions. · Lead CTM supply chain activities starting with collabora ...

This position supports Supplier Quality Assurance with activities related to supplier qualification and regulatory compliance. · Manage initial intake of new regulated suppliers from the business teams · Conduct or assist with supplier risk assessments · ...

HAYA Therapeutics is seeking a senior-level Scientific Computing / SysOps / DevOps consultant to bridge the gap between IT operations and scientific discovery. · ...

The Clinical Study Manager III will be responsible for working collaboratively with the development team to establish clinical development plans and design/executing protocols for studies included in the development plan. · ...

This position is responsible for the regulatory lifecycle management of oncology clinical trials. · Prepares and submits research plans protocols and regulatory documents to the IRB. · Drafts Informed Consent Documents (ICDs) translating complex medical procedures risks into layp ...

Faro Health aims to improve lives by helping life sciences companies answer complex clinical questions simply efficiently and effectively. Our software platform is used to orchestrate complex clinical development with a single source of truth empowering researchers to design more ...

We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. · The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with ...

The Clinical Solutions Specialist (Part Time) supports the success of the Faro platform by contributing to study modeling and data-driven feature improvements. This role involves interpreting clinical protocols and modeling studies in the Faro platform across various therapeutic ...

The Clinical Device Data Specialist is responsible for ensuring the quality and integrity of device data. · ...

The Clinical Project Manager is responsible for managing and executing clinical studies from study initiation through study closeout, as well as assuring compliance with regulatory and quality procedures and standards. · Coordinate and supervise study execution and contract manag ...

Piper Companies es buscado por un Master Linux System Administrator para unirse a contratista gubernamental trabajando en San Diego CA. Un secreto activo clearance y la capacidad para trabajar en sitio en Point Loma son necesarios para la consideración Este es una oportunidad de ...