Collecting information
Organizing data
Under general supervision of a licensed practitioner and/or department leader, the Clin-Med Assist I independently provides and documents clinical care and associated tasks as assigned and as per standardized clinical protocols. Advanced knowledge of medical terminology; experience with data entry a
Good knowledge of applicable clinical research regulatory requirements including Good Clinical Practice and International Conference on Harmonization guidelines. Perform clinical monitoring activities to ensure that the clinical studies are conducted, recorded, and reported in accordance with the pr
The Senior Medical Affairs Operations Manager is responsible for managing the execution of medical affairs operations, investigator initiated clinical studies, post-marketing clinical studies and post-trial access programs. Senior Medical Affairs Operations Manager page is loaded## Senior Medical Af
Perform clinical monitoring activities to ensure that the clinical studies are conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures, Good Clinical Practice, and applicable regulatory requirements. Good knowledge of applicable clinical research regulatory r
AHA Basic Life Support for Healthcare Professional (AHA BLS Healthcare) - American Heart Association -REQUIRED. California Registered Nurse (RN) - CA Board of Registered Nursing; AHA Basic Life Support for Healthcare Professional (AHA BLS Healthcare) - American Heart Association. Clinical leadership
A strong foundation in medical writing and regulatory submissions is essential, alongside effective communication skills. A biopharma consultancy is seeking an MWS Consultant I to lead the authoring of regulatory documents and manage projects.
Provide clinical leadership and lead clinical communication to upper management on trial issues, patient recruitment, investigator's feedback, patient enrollment issues and present a plan of action for resolution of issue* Author and/or review clinical documents required for the conduct of clinical
A leading pharmaceutical company is seeking a Senior Medical Affairs Operations Manager to oversee the execution of clinical studies and manage the medical affairs operation. The role requires managing clinical protocols, leading teams, and ensuring compliance with regulatory standards. Candidates s
A prominent healthcare organization is seeking a Vice President of Clinical Data & Analytics to lead the clinical analytics vision and strategy. Candidates should have 15+ years of relevant experience and a strong background in healthcare analytics, along with expertise in statistical methods and te
At the direction of Medicare program leadership, supports portfolio management and/or initiative-specific change and project management. Experience with Medicare programs. Molina Healthcare offers a competitive benefits and compensation package.
The ideal candidate has 10 years of experience in Regulatory Affairs within the biopharmaceutical industry, including supervisory roles. A biopharmaceutical company in San Diego seeks an Associate Director, Regulatory Affairs CMC. This role focuses on regulatory strategy execution for drug developme
The Senior Medical Director, Clinical Research will be working within a multi-disciplinary team and will be accountable for developing the strategy and the Clinical Development Plan for one or more indications for a specific Crinetics' compound. Support advisory boards, key opinion leader engagement
A leading pharmaceutical company is seeking a Vice President of Clinical Research Endocrinology to lead strategic clinical initiatives. Candidates should possess extensive experience in clinical research, strong communication skills, and an MD degree with relevant endocrinology expertise. This is an
Summary The Vice President, Clinical Data & Analytics is an enterprise leader responsible for defining and executing MedImpact’s clinical analytics vision: Proactive, Individualized, Whole-Person, and Sustainable/Scalable Care. Lead development of an enterprise clinical analytics roadmap that unif
Per standardized clinical protocols, independently provides and documents clinical care and associated tasks as assigned. Under the general supervision of a licensed care provider and/or management, the Clinical Medical Assistant I (CMA I)/ Patient Access Representative II (PAR II) is responsible to
Provide regulatory assistance and review of clinical study documentation, including review of clinical protocols, informed consent documents, clinical study recruitment materials, and essential document packages. Associate Director, Regulatory Affairs CMC page is loaded## Associate Director, Regulat
California Registered Nurse (RN) - CA Board of Registered Nursing - REQUIRED AHA Basic Life Support for Healthcare Professionals (AHA BLS Healthcare) - American Heart Association - REQUIRED Essential Functions Clinical advancement: Uses systematic planning, appropriate methods and timely exchange of
A leading pharmaceutical company in San Diego seeks a Senior Medical Director to lead clinical research initiatives. Ideal candidates will have an MD and over 10 years in biopharma, including experience in clinical trial execution and regulatory interactions. This role involves developing clinical s
A healthcare company is offering an internship program in San Diego, California, to provide students with real-world experience in Medical Affairs, particularly in artificial intelligence applications in healthcare. Interns will assist with research projects and scientific publications, conduct lite
A leading academic medical institution in San Diego is seeking an Administrative Coordinator for the Center for Clinical Research. The ideal candidate will manage multiple tasks, communicate effectively, and have a background in clinical trials management. This role requires strong organizational an