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The Medical and Assistant and Patient Care Representative is responsible for patient flow, communication, and scheduling, while supporting a seamless, patient-focused clinical environment that reflects Dermacare's high standards of care. Dermacare's clinical, patient care duties, and Front Desk supp
Vice President, Regulatory Affairs, Clinical Operations & Medical Affairs. The Company is in search of a Vice President for Regulatory Affairs, Clinical Operations, and Medical Affairs. A minimum of 10 years' in regulatory affairs leadership is required, along with significant experience in overseei
Under the direct supervision of a licensed care practitioner, the Patient Care Assistant II provides and documents clinical care and associated tasks as assigned. Regularly performs a supportive role to physicians nurses and families in the delivery of patient care by assisting patient care delivery
Scripps Memorial Hospital La Jolla has been one of Southern California's premier medical centers for more than 90 years and has been consistently recognized for quality patient care and the first hospital in San Diego to be designated a Magnet Hospital by the American Nursing Association for excelle
Jobboard is seeking an Associate Director of Regulatory Affairs to provide regulatory support for medical device systems at our San Diego site. The ideal candidate will have over 10 years of experience in the Medical Device industry and at least 5 years in Regulatory Affairs. This role involves deve
Prepare and deliver high-quality and timely regulatory submissions in compliance with applicable regulatory requirements. In this role, you will collaborate closely with colleagues across regulatory operations, quality, CMC, nonclinical and clinical functions to support high-quality, timely regulato
The Senior Director, Regulatory Operations provides strategic and operational leadership for global regulatory operations, overseeing electronic submissions, regulatory information management systems, and end-to-end submission execution. This role is a key member of the Global Regulatory Affairs Lea
The Manager, Medical Writing Operations is responsible for leading document specialist support across the Medical Writing function and for authoring and coordinating regulatory, clinical, and safety documents. Partner with Medical Writing, Regulatory Operations, Clinical Development, Biometrics, Pha
To qualify for the Regulatory Affairs Specialist III role, candidates must have a Bachelor's degree in life sciences, engineering, or a related field, along with at least 6 years of experience in a regulated environment, including 4 years of direct experience in Regulatory Affairs. The Regulatory Af
Design, develops, and enculturates innovative ways to transform nursing care delivery and patient care systems Serves as the professional practice resource for the Patient Care leadership and Shared Governance councils, supporting the integration of professional practice standards into performance i