Regulatory Coordinator: Average Salary in Redwood City, CA in 2024

Minimum 10 years of professional experience with production and/or construction administration of architectural projects, including freestanding Type I buildingsSome California healthcare project experience ideal. Plan, design, and organize internal work for healthcare-focused projects throughout al...

Responsible for reporting monthly adjustments and corrections to the Compliance Manager. ...

As the Technical Project Manager you will be the technical resource assigned to a number of projects in coordination with the project managers. As a Technical Project Manager, you will work with the project team to provide technical expertise during key parts of the deployment process. Work with Pro...

The Compliance Specialist will collaborate with the Compliance Team and Quality/Compliance Manager to develop procedures, policies, and best practices that ensure the company operates within legal and ethical guidelines. Additionally, they will work with the Compliance team to handle customer survey...

The Clinical Program Manager – Oncology, EMEA will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required. At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, inclu...

The Configuration Management Technical Program Manager (TPM) in PMO is an experienced cross-functional program management leader that will be responsible for planning and execution of technical and integrated product milestones for our vehicle platforms. The Program Management Office (PMO) at Zoox i...

Document management including uploading and tracking regulatory files, archival of regulatory correspondences and maintenance of regulatory submission log according to established procedures. The individual will represent Regulatory Affairs and work closely with cross-functional teams and external p...

Plan, organize, coordinate, and inspect all Capital Projects. Inspect, generate punch lists, and sign off to accept new construction projects. Coordinate vendors to meet deadlines in the completion of Capital Projects. ...

Reporting to Clinical Research Manager for Sarcoma Oncology, the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to manage data, enroll and follow patients on trial and assist with regulatory and financial r...

We are currently looking for a Clinical Research Coordinator Associate to assist with translational research efforts. As a Clinical Research Coordinator Associate, you would coordinate various aspects of clinical studies, such as but not limited to recruiting participants, preparing study procedures...

We are looking for a Project/Supply Chain Coordinator to work for a growing team within a Network PMO group. ...

The IT Compliance Analyst will be responsible to execute the annual Audit Plan which will consist of assessing the design and effectiveness of controls, accuracy of data and records, effectiveness of operations, as well as ensuring the compliance of established policies, rules, and regulations. The ...

Associate Director, Regulatory Affairs Advertising and Promotion. Regulatory Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across cross-functional teams. Significant experience contributing t...

Client is looking for consultant who can join Risk, Compliance & Integrity organization and can brings together critical compliance, assurance, risk and governance functions across and help the company meet compliance needs and enable our businesses to innovate. Assess and advise stakeholders on com...

Principal Regulatory Affairs Specialist. Responsibilities also include keeping senior management informed of regulatory status of products and significant regulatory issues as well as maintain proficiency in global regulatory requirements. Proven expertise in all aspects of Regulatory Affairs; Strat...

Assist in the preparation of regulatory submissions in support of IVDR implementation of Toxicology and Therapeutic Drug Monitoring Assays. Tasks include:o Organize and assist in the review of materials for inclusion in regulatory submissions both in the EU and worldwide. Support the preparation of ...

LEGARZA PROGRAM SPECIALIST - FULL TIME AND PART TIME POSITIONS AVAILABLE. We are in search of a motivated go-getter who has the skills and determination to develop, grow, and manage a phenomenal sports program. As we continue to expand, we need a quality person who believes in our values and has the...

Project Coordinators own key phases of the Interior Design Project lifecycle and contribute to the success of RH Interior Design by supporting our Lead Designers. Create and maintain comprehensive project and design documentation. Coordinate initial phases of interior design projects, including cons...

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. Experience with Japanese and Chinese regulatory submissions. Ability to interpret and apply regulatory requir...

Under direction, the Program Services Coordinator assists in the planning, coordination, and implementation of services, such as student recruitment, orientation, job skills assessments and job placement, special events, tours, individual and specialized programs and other support for current and po...

The IT Project Manager will oversee the procurement, planning, execution, and implementation of the Regional Medical Center (RMC) project and may assist with current projects to allow in-house staff to focus on implementation. Ability to track project tasks to execution and work with department mana...

The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...

Staff Technical Program Manager. Option 1: Bachelor’s degree in computer science, information technology, engineering, or related area and 5 years’ experience in engineering, engineering program management, technical program management, product management, or related area. Option 2: 7 years’ experie...

Apply fast, check the full description by scrolling below to find out the full requirements for this role.As one of the first pioneers of earned wage access, our passion at EarnIn is building products that deliver real-time financial flexibility for those with the unique needs of living paycheck to ...

The Project Coordinator in the Administration department is responsible for managing resources and controlling mid to large scale medical equipment and estate related projects. A project coordinator leads activities related to product and/or equipment selection and standardization as per clinical re...