Collecting information
Organizing data
Coordinate and collaborate regulatory activities across functions within ORIC, ie, regulatory operations, quality, CMC, nonclinical, clinical. Excellent writing and editorial skills, ability to collaborate on development of high‑quality clinical‑regulatory documents, eg, investigator brochures,
Integrates scientific, clinical, safety, and commercial considerations to build cohesive regulatory roadmaps from first-in-human through post-marketing lifecycle management. The Executive Director, Regulatory Strategy – Endocrinology is a senior regulatory leader responsible for shaping and drivin
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
The Associate Director, Regulatory Affairs Project Planning & Coordination is responsible for developing, implementing, and monitoring project plans and best practices that facilitate how the Global Regulatory Affairs department executes its strategic and functional goals. Support Global Regulatory
Promotes clinical effectiveness, efficient use of resources, and quality care in practice setting. Facility:** Sharp Memorial Hospital. Clinical advancementUses systematic planning, appropriate methods and timely exchange of information with multidisciplinary team and patient/family to coordinate ca
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
Identify, develop, and close new business opportunities within Veterans Affairs Medical Centers (VAMCs), Community Based Outpatient Clinics (CBOCs), and affiliated healthcare systems. We are an ISO 13485 certified company committed to providing high-quality medical solutions that consistently meet c
Support Delta Medical Systems' quality policy through compliance with quality management system documentation. The Associate Representative is designed for individuals early in their career in sales and the medical industry. At Delta Medical Systems, we are collaborative, empowered,.
MillenniumSoft Inc is seeking a Senior Systems Engineer in San Diego, CA, to lead the development of innovative medical device solutions. This remote role requires expertise in Systems Engineering and proven leadership in managing multi-disciplinary teams.
Support Delta Medical Systems' quality policy through compliance with quality management system documentation. Working closely with a mentor Product Sales Executive, the PSA gains hands‑on exposure to the full sales lifecycle while learning how to identify customer needs, support the development o
Advanced knowledge of medical terminology; experience with data entry and clinical computer systems. Under general supervision of a licensed practitioner and/or department leader, the Clin-Med Assist II independently provides and documents clinical care and associated tasks as assigned and as per st
Manager, Trial Disclosure, Medical Writing Operations page is loaded## Manager, Trial Disclosure, Medical Writing Operationsremote type:. Education and Experience:**Required:* Bachelor’s Degree required; advanced degree in life sciences, public health, regulatory science, or related discipline pre
A pharmaceutical company in San Diego seeks a Manager of Medical Writing Operations for Trial Disclosure. This role is integral to clinical trial transparency, responsible for ensuring compliance with disclosure regulations. You will work in collaboration with cross-functional teams, develop content
Position Summary:**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#
Advanced knowledge of medical terminology; experience with data entry and clinical computer systems. 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 sta
The Clinical Procedure Sales Representative is responsible for promoting and selling Clinical Procedure productsincluding Peripheral IV Access, Pain Control, IV Anesthesia Sets, and Regional Anesthesiaalong with related services. Many of our customers and potential customers are in clinical settings
MedSchoolCoach is seeking a part-time Student Support Auditor to join its quality assurance team. The ideal candidate will have a medical background and possess strong analytical skills and attention to detail.
Associate Director, Regulatory Affairs CMC page is loaded## Associate Director, Regulatory Affairs CMCremote type:. Maintain effective interactions with all contributors and Regulatory Affairs management, to ensure timely delivery of documents for regulatory submission. Provide regulatory assistance
Position Summary:**The Senior Manager, Clinical Data Management – External Data Management (CDM‐EDM) is a hands‐on, individual contributor role responsible for executing and owning external (non‐EDC) data management activities for assigned clinical studies. Senior Manager, Clinical Data Mana
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