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

The Coordinator, Regulatory is responsible for maintaining procedures and fulfilling daily administrative responsibilities in the Regulatory Affairs Department to ensure compliance of all new and existing products. The Coordinator, Regulatory will assist in providing regulatory support to cross-func...

Who are we and why should you join us?.BetterHelp is on a mission to remove the traditional barriers to therapy and make mental health care more accessible to everyone.Founded in 2013, we are now the world's largest online therapy service - providing affordable and convenient therapy in 210 countrie...

Who are we and why should you join us?BetterHelp is on a mission to remove the traditional barriers to therapy and make mental health care more accessible to everyone.Founded in 2013, we are now the world's largest online therapy service - providing affordable and convenient therapy in 210 countries...

Work with the program assistant as a program Coordinator monitor program budget; purchase needed materials, write applications for small grants. Work with the program assistant to coordinate Advisory Board meetings and attend other program related meetings such as VTEA, write program review and accr...

From these plans, the Project Manager will coordinate internally with Engineering, Development, and Operations to fulfill projects on time and within the project budget. As the Project Manager you will be the liaison between Engineering and Technical Sales to document and refine product requirements...

II) supervision general direction, designs and develops program activities, objectives, and procedures pursuant to District, state, and/or federal regulations and guidelines; monitors and coordinates the delivery of program services; develops and administers program budget; applies for and administe...

The Associate Director, Regulatory Affairs will be responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines. Must have an extensive knowledge of regulatory requirements, including ICH and regional requirements, and have an under...

Partner with business Project Managers and Vendor Project Managers to leverage organizational tools for effective project and program management. We are seeking an experienced IT Program Manager responsible for driving scalable solutions in Business Applications through strategic planning and execut...

Clinical Research Coordinator 2 (Fixed-term 2 years) to conduct clinical research and work independently on progressively more complex projects/assignments. Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. The Department of Anesthe...

Clinical Research Coordinator with project management skills for research on healthy aging, Parkinson’s disease, and aging with HIV infection. Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. We are looking for a Clinical Research ...

The Kwo Lab is seeking a Clinical Research Coordinator II (CRC2) to provide support for clinical research efforts in the Division of Gastroenterology and Hepatology. Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. Determine effect...

We are supporting a small growing biotech in the Bay Area looking for a Senior Regulatory Affairs Associate!. Atleast 2 years experience in a regulatory setting at a biotech company. Strong foundation in biological or physical sciences, with the ability to apply scientific knowledge to regulatory ma...

Responsible for overall coordination between US-based customers and global GoerTek teams, you will interact with customer operations, CAPEX, and engineering teams daily, and be responsible for driving schedules and deliverables from GoerTek teams in China.Coordinate the responsibility for Product De...

Job Description: Regulatory Affairs Specialist. Provide consultation and advice to regulatory specialists regarding change control and product development. Contribute to continuous improvement initiatives within the regulatory affairs function. Ability to interpret and apply regulatory requirements....

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...

Compliance & Ethics Specialist. Perform field and desk monitoring to ensure compliance with to relevant laws and regulations. Track, analyze, and report on compliance monitoring progress, identifying trends and potential risks. Provide compliance guidance and support for various initiatives and proj...

A degree in a life science, chemistry, or chemical engineering or closely related discipline with a graduate degree preferred and at least 10 years of experience in pharmaceutical regulatory affairs, that includes, but cannot be limited to, CMC regulatory affairs. Associate) Director, Regulatory Aff...

Apex Systems is seeking a Clinical Research Coordinator to support data collection in the lab. Coordinate clinical technology validation studies, leading operational planning and day-to-day management of research execution. Serve as primary contact with research participants, vendors, and research l...

The project coordinators main role is to assist the Senior Project Lead of GoodShop with:. Interfacing with clients, vendors and design team to ensure all project deadlines are met. Organization of past and current projects. Project Management experience preferred. ...

Title: SAP Finance Project Manager. Intermediate level project manager. Publish project status, organize project docs. Create and manage Project Plans. ...

Should be responsible (and have had a demonstrated capability) for developing detailed project plans, ensuring resource availability and allocation of every project. Ensure the completion of all projects are delivered on-time, within scope and to the right level of expectations and specifications. C...

We are currently seeking a Senior Regulatory Affairs Specialist to drive regulatory strategies and submissions for medical devices. Senior Regulatory Affairs Specialist. Hands-on experience with major regulatory submissions and managing interactions with regulatory agencies. Develop and implement gl...

Assist the field Clinical Development team with administrative tasks for all clinical trials, including tracking study status and enrollment, managing research budgets, and maintaining up-to-date regulatory documents as required. Coordinate and organize clinical staff resources for internal research...

Our client has a unique opportunity for a highly skilled Principal Regulatory Specialist to join a growing team working on novel technology in the Neurological/Spine space. Lead regulatory strategy and submissions for Class 2 & 3 products, including PMA and 510(k) applications. Develop and execute r...

Apple is looking for a dynamic, highly motivated Program Manager to join the WW Channel Sales Finance team. Note: Apple benefit, compensation and employee stock programs are subject to eligibility requirements and other terms of the applicable plan or program. Work closely with Business Process Re-E...