Regulatory Associate: Average Salary in National City, CA in 2024

A company is looking for an Associate Director, Global Regulatory Project Management and Strategic Planning - GI. ...

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. The...

A company is looking for a Regulatory Consulting Associate responsible for preparing plan documents and providing regulatory compliance support. ...

Work closely with the Director, Regulatory Ad Promo to formulate the strategic direction and develop process improvements for the Regulatory Ad/Promotion function. Independently represents Regulatory Affairs on the Medical Review Committee (MRC) and be responsible for conducting the regulatory revie...

A company is looking for an Associate Director, Regulatory Affairs and Submissions. ...

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...

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

The Associate Director of Regulatory Affairs will play a crucial role in leading and managing the regulatory submissions for CorDx medical device products, including 510(k) and De Novo submissions. Job Title: Associate Director of Regulatory Affairs. Conduct regulatory assessments for product change...

Associate Director, Regulatory Affairs, CMC. This position is responsible for assigned regulatory projects to ensure regulatory compliance for approved marketing applications (NDA/MAA/NDS etc. It also provides regulatory expertise to the Regulatory team. Work with submission manager to ensure regula...

The Associate Director, Regulatory Affairs is responsible for establishing regulatory strategies in coordination with departmental leadership, and independently managing life cycle plans along with regulatory submissions and approvals. Comprehensive knowledge of current US and ex-US regulations and ...

Develop, implement, and update procedural and training manuals for the Regulatory Associates and Regulatory Department. Work closely and collaboratively with clinical project management staff to plan and delegate collaborative tasks for study coordinators and regulatory associates to ensure completi...

The Regulatory Associate will primarily focus on provider reimbursement issues, Medicare and Medicaid appeals, and audits and internal investigations, supporting the firm's robust and sophisticated regulatory and reimbursement practices. A leading national healthcare law firm is seeking a Regulatory...

Work closely with the Director, Regulatory Ad Promo to formulate the strategic direction and develop process improvements for the Regulatory Ad/Promotion function. Independently represents Regulatory Affairs on the Medical Review Committee (MRC) and be responsible for conducting the regulatory revie...

The Associate Director of Regulatory Affairs will play a crucial role in leading and managing the regulatory submissions for CorDx medical device products, including 510(k) and De Novo submissions. Job Title: Associate Director of Regulatory Affairs. Conduct regulatory assessments for product change...

Corporate/Regulatory Associate. Our corporate/commercial health practice offers general counsel, health regulatory and governance advice to healthcare organizations, associations and professionals. We provide strategic advice and regulatory opinions on a wide variety of issues. ...

A company is looking for a Senior Ethics and Compliance Specialist to join their Corporate Compliance team. ...

Specialist Product Training Compliance to support the Structural Heart Global Training and Education team. ...

A company is looking for a Senior Manager, Regulatory Affairs IVD & CDx. ...

A company is looking for a Regulatory Affairs Senior Associate to support regulatory document management and clinical trial submissions. ...

A company is looking for a Compliance Analyst III to conduct transaction monitoring investigations and ensure regulatory compliance. ...

Family Health Centers of San Diego is looking for a Coding Compliance Specialist to perform audits of coding and billing, ensuring compliance with department, state, and federal rules and requirements. May spend a portion of time coding and abstracting clinic medical records, for the purpose of reim...

A company is looking for a Creative Manager/Project Manager to lead the production and execution of large-scale marketing campaigns. ...

A company is looking for a Tax Compliance Specialist with at least 1 year of experience in tax compliance and accounting. ...

Key Responsibilities:Develop and implement regulatory strategies for global medical device clearances and approvalsManage regulatory submissions and communications with FDA and EU notified bodiesProvide regulatory guidance to cross-functional teams throughout the product lifecycleRequired Qualificat...