Regulatory Coordinator: salario promedio en Irvine, CA in 2024

Under the supervision of the Regulatory Program Manager (RPM) of the Regulatory Affairs Unit, the Regulatory Affairs Coordinator (RAC) supports the clinical research efforts of the Chao Family Comprehensive Cancer Center by providing comprehensive, regulatory management of cancer-related protocols i...

Five (5) years of regulatory documentation experience in clinical research required. Working knowledge of NIH, and OHRP regulatory requirements and ICH GCP guidelines preferred. ...

The Assistant Regulatory Affairs Coordinator position will work directly with the Lead Regulatory Coordinator to ensure successful management of the regulatory aspects of each study conducted through UCI's Center for Clinical Research. ...

Regulatory Coordinator ensures all research studies are compliant with regulations and maintains accurate and up-to-date regulatory files. Clinical Research Regulatory Coordinator supports clinical research teams (physicians, nurses, etc. Coordinator is the central resource for regulatory staff cond...

Regulatory Coordinator ensures all research studies are compliant with regulations and maintains accurate and up-to-date regulatory files. Clinical Research Regulatory Coordinator supports clinical research teams (physicians, nurses, etc. Coordinator is the central resource for regulatory staff cond...

Regulatory Coordinator ensures all research studies are compliant with regulations and maintains accurate and up-to-date regulatory files. Clinical Research Regulatory Coordinator supports clinical research teams (physicians, nurses, etc. Coordinator is the central resource for regulatory staff cond...

Regulatory Coordinator ensures all research studies are compliant with regulations and maintains accurate and up-to-date regulatory files. Clinical Research Regulatory Coordinator supports clinical research teams (physicians, nurses, etc. Coordinator is the central resource for regulatory staff cond...

Clinical Research Coordinator, CRC, Clinical Research, Clinical Trials, Phlebotomy, Blood, Blood Draw, Draw Blood, Therapeutic, Human Trials, Phases I-IV, Oncology, Cancer Trials, Oncology Research, Regulatory Affairs, Phase I, Phase II, Phase III, Good Clinical Practice, GCP, Regulatory, Clinical T...

Q-SYS Professional Services Project Manager. The Professional Services Project Manager will provide best-in-class task and timeline management for multiple complex Q-SYS programming engagements simultaneously. The Professional Services Project Manager will work closely and collaboratively with Profe...

Under the direction of the Principal Investigator and Program Manager, the Clinical Research Coordinator supports the efforts of several research projects, including regional projects and national clinical trials with the opportunity to interface with local and national level leaders in medicine and...

Under the supervision of the Assistant Director of Clinical Research Operations, the incumbent is responsible for coordinating clinical trials in the UCI Center for Clinical Research (CCR). The UCI Center for Clinical Research (CCR) is driven to improve health and wellness of people in Orange County...

Start Date: ASAPThe Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site manag. Title: Clinical Research Coordinator. ...

Under supervision of the Clinical Research Manager of the Clinical Trials Unit, the Assistant Clinical Research Coordinator supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management of multiple Phase II-IV cancer-related protocols accordi...

Under general supervision of the Assistant Program Director and the Program Manager of the Pediatric Residency Program in the Department of Pediatrics at UC Irvine the incumbent is responsible for providing a wide range of general administrative and financial support to the program. Led by Chancello...

The Program Coordinator will play a critical role in driving the strategic initiatives of the Center and conduct research activities to further the Center's mission and growth. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs. This position inv...

The role of the Stroke Program Coordinator is one of educator, collaborator, consultant, and change agent. Category:Healthcare, Keywords:Healthcare Program Coordinator, Location:Santa Ana, CA-92702. The primary responsibilities are to drive quality, improve clinical outcomes, and facilitate programm...

A leading provider in the health care and digital health space is seeking a Senior Regulatory Affairs Specialist to join their regulatory team. Minimum of 5 years of experience in medical device Regulatory Affairs with a deep understanding of regulatory frameworks. As a key player in regulatory over...

Job Description: Regulatory Affairs Specialist - On-site 5x a week in Alameda, CA. Provide consultation and advice to regulatory specialists regarding change control and product development. Contribute to continuous improvement initiatives within the regulatory affairs function. Experience with Japa...

As an Associate Director of Regulatory Affairs, you will represent regulatory affairs on cross-functional teams and provide regulatory advice on clinical development matters. Associate Director, Regulatory Affairs. Regulatory Affairs, regulatory submissions, drug development, oncology, FDA, EMA. Fun...

Associate Director Regulatory Affairs (Temp to Perm). Oversee regulatory submissions and approvals, ensuring alignment with global regulatory standards. Regulatory Affairs, including. Lead regulatory strategy development and execution for both U. ...

Lead the String Authoring Rollout Program: Work with the Rollout Program Core Team to come up with an action plan on how to complete the rollout program (i. Job Title: Program Coordinator III. The project coordinator is responsible for managing strategic aspects of client and company projects, track...

This Associate Director of Regulatory CMC will directly report to the Senior Director of Regulatory Affairs, CMC, and will be responsible for representing regulatory CMC on cell therapy pipeline + products. Associate Director, Regulatory Affairs CMC. Regulatory Affairs CMC experience in a pharma/bio...

As a Senior Associate of Regulatory Affairs, you will support Regulatory Affairs management in the day-to-day operational aspect of the department and support interactions with global regulatory authorities. Senior Associate, Regulatory Affairs. Represent Regulatory Affairs on project teams and clos...

Senior Regulatory Affairs Specialist. Draft, edit, and compile technical documentation and design dossiers to support CE mark/UKCA mark regulatory filings. Prepare regulatory submissions for FDA 510(k) clearance and A2F submissions. Research regulatory requirements from FDA, CMDR, MDR, IVDR, and UK ...

Reporting into the Deputy Head of Global Compliance (HOC), the Senior Regulatory Compliance Program Analyst is responsible for supporting the implementation and ongoing oversight of the global Compliance regime including but not limited to performing regulatory filings, assisting with independent re...