Regulatory Affairs Associate

Job DescriptionJob DescriptionFoster City, CAContract Duration: 6-18 monthsRate: NegotiableResponsibilities:Excellent employment opportunity for a Regulatory Affairs CMC Associate in the Foster City, CA area. Bay area candidates ONLYProvide Regulatory CMC support for biologic and small molecule drugs being evaluated or marketed for the treatment of oncology,...

Description Home Search Jobs Job Description Regulatory Affairs Associate - II Contract: Foster City, California, US Salary: $60.00 Per Hour Job Code: 352568 End Date: 2024-09-08 Days Left: 28 days, 3 hours left Apply Pay range: $55 to $50/hr.Responsibilities: Collaborate with the RA CMC team to meet deliverables and timelines Ensure data...

Job Title: Regulatory Affairs CMC – Data Administrator ContractorLocation: Foster City, CA 94404Duration: 12+ Months (Extendable)Pay Rate: $65.00/hr. on W2Specific Job Responsibilities:Perform data entry using Information Systems to enter and maintain relevant product information to support cross-functional stakeholders.Work collaboratively to support the...

Job Title: Regulatory Affairs CMC – Data Administrator ContractorLocation: Foster City, CA 94404Duration: 12+ Months (Extendable)Pay Rate: $65.00/hr. on W2Specific Job Responsibilities:Perform data entry using Information Systems to enter and maintain relevant product information to support cross-functional stakeholders.Work collaboratively to support the...

Overview: Prefers the candidate to be local in the Bay Area BUT will consider qualified candidates with Pharma Regulatory CMC experience in the Pacific time zone ONLY. Responsibilities Responsible for the preparation of moderately complex regulatory submissions which require interaction with departments outside of Regulatory Affairs CMC for investigational...

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap –...

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap –...

The Regulatory Affairs CMC (Chemistry, Manufacturing, and Controls) – Data Administrator Contractor will play a key role in supporting the RA CMC team by managing product information within Gilead Information Systems. This position involves routine data entry, quality control, and report generation to ensure the completeness, correctness, and consistency...

Position Summary:   Reporting to the SVP, Regulatory Affairs, the Senior Manager or Associate Director of Regulatory Affairs will lead and participate in regulatory activities associated with IND/CTA preparations and maintenance to support new and ongoing development programs. This role requires an independent, self-directed, and highly motivated...

Position Summary:Reporting to the SVP, Regulatory Affairs, the Senior Manager or Associate Director of Regulatory Affairs will lead and participate in regulatory activities associated with IND/CTA preparations and maintenance to support new and ongoing development programs. This role requires an independent, self-directed, and highly motivated regulatory...

Position Summary:Reporting to the SVP, Regulatory Affairs, the Senior Manager or Associate Director of Regulatory Affairs will lead and participate in regulatory activities associated with IND/CTA preparations and maintenance to support new and ongoing development programs. This role requires an independent, self-directed, and highly motivated regulatory...

Position Summary:Reporting to the SVP, Regulatory Affairs, the Senior Manager or Associate Director of Regulatory Affairs will lead and participate in regulatory activities associated with IND/CTA preparations and maintenance to support new and ongoing development programs. This role requires an independent, self-directed, and highly motivated regulatory...

The KYDA Partners team is seeking a Regulatory Affairs Manager to lead and manage the regulatory affairs department, ensuring compliance with regulatory standards and the quality management system.Key Responsibilities:Internal Audits:Review and approve audit agendas, plans, and summary reports.External Audits:Facilitate and participate in external...

The KYDA Partners team is seeking a Regulatory Affairs Manager to lead and manage the regulatory affairs department, ensuring compliance with regulatory standards and the quality management system.Key Responsibilities:Internal Audits:Review and approve audit agendas, plans, and summary reports.External Audits:Facilitate and participate in external...

Join Our Team as a Regulatory Affairs ManagerWe are seeking a skilled Regulatory Affairs Manager to become part of our client's team and have a significant role in introducing new products to the market. As the Regulatory Affairs Manager, you will be responsible for leading the regulatory strategy and overseeing submissions for new product releases within...

We are looking for a talented Regulatory Affairs Manager to join our client's team and play a crucial role in bringing new products to market. This role will be responsible for leading the regulatory strategy and managing submissions for new product launches for our client's cardiovascular medical device portfolio. This hands-on role requires a...

Job DescriptionJob DescriptionSalary: $90KPurpose:The Regulatory Affairs Manager is responsible for managing the regulatory affairs department and functions to ensure regulatory compliance of quality management system.Duties & Responsibilities: Review and approve audit agenda, plan, summary reports for internal audits. Facilitate and participate in external...

Job Description Job Title: Regulatory Affairs Specialist Company: US Tech Solutions Job type: Contract Duration: 12 months ID: 5175 Department: Regulatory Affairs Prerequisites: BS/BA degree in Scientific Discipline (Masters or higher preferred) A minimum of 7 years in the pharmaceutical industry A minimum of 5 years CMC regulatory (biologics preferred)...

An exciting and innovative clinical-stage biopharmaceutical company dedicated to the development of first-in-class cellular immunotherapies for patients with cancer and autoimmune disease is looking for an Associate Director in Regulatory Affairs to oversee and contribute to the strategic planning and execution of clinical regulatory activities essential for...

An exciting and innovative clinical-stage biopharmaceutical company dedicated to the development of first-in-class cellular immunotherapies for patients with cancer and autoimmune disease is looking for an Associate Director in Regulatory Affairs to oversee and contribute to the strategic planning and execution of clinical regulatory activities essential for...