Collecting information
Organizing data
Coordinate and collaborate regulatory activities across functions within ORIC, ie, regulatory operations, quality, CMC, nonclinical, clinical. This involves working closely with cross‑functional colleagues including regulatory operations, quality, CMC, nonclinical and clinical team members. Lead t
ORIC Pharmaceuticals is seeking a Director/Associate Director in Regulatory Affairs to support clinical development of oncology products. This role requires at least 8 years of regulatory affairs experience and excellent communication skills. The successful candidate will support regulatory submissi
Responsible for the regulatory CMC leadership of one or more commercial and development projects, including responsibility for regulatory strategy, IND/CTA preparation, maintenance and update activities, interaction with and preparation for key milestone meetings with regulatory agencies with focus
Partners closely with Clinical Development, Safety, Commercial, CMC, Quality, and Legal to ensure aligned and value-generating regulatory strategies. Ability to synthesize scientific, clinical, safety, and business inputs into cohesive regulatory strategy. This role requires a highly strategic, scie
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
Sharp HealthCare in San Diego, California, seeks a Registered Nurse (RN) to provide nursing services to patients and families. The role requires a California RN license, with a minimum of 3 years of clinical experience and AHA Basic Life Support certification. Candidates will engage in diverse respo
Masters or doctoral prepared nurse with Clinical Nurse Specialist Certificate who applies clinical expertise in evidence-based nursing practice within three spheres of influence; 1) patient/client, 2) nurses/nursing practice, and 3) organization/system in the following roles: clinical expert, educat
A bachelor’s degree with a minimum of 12 years of GCP quality assurance experience, a master’s degree with a minimum of 8 years of relevant experience, a PhD with a minimum of 5 years of relevant experience, or an equivalent combination of education and experience is required with a healthcare/s
Neighborhood Healthcare in Escondido is seeking a Risk Manager to promote risk management and patient safety across the organization. This role offers the chance to work in a community health setting and make a significant impact on patient safety and risk exposure. The ideal candidate has extensive
Deep clinical domain knowledge including understanding of clinical workflows, medical terminology, and healthcare delivery processes. Cross-functional Collaboration: Partner with data engineers, clinical advisors, and product teams to ensure technical implementations align with clinical requirements
Job Details Profession: Non-Clinical - Administrative Pay: $961.
Partners closely with Clinical Development, Safety, Commercial, CMC, Quality, and Legal to ensure aligned and value-generating regulatory strategies. Ability to synthesize scientific, clinical, safety, and business inputs into cohesive regulatory strategy. This role requires a highly strategic, scie
Responsible for the regulatory CMC leadership of one or more commercial and development projects, including responsibility for regulatory strategy, IND/CTA preparation, maintenance and update activities, interaction with and preparation for key milestone meetings with regulatory agencies with focus
The ideal candidate will assist with medical record audits, data collection, and performance improvement initiatives to enhance patient safety and regulatory compliance. Aurora San Diego Hospital is seeking a Quality Coordinator to support the Quality and Risk Management Department.
The ideal candidate will advise on company clinical quality strategy, ensure compliance to regulations, oversee quality management systems and interact directly with cross functional clinical, regulatory and quality teams. The Manager/Senior Manager of Clinical GCP Quality will be responsible for ev
The Associate Director, Quality Operations plays a critical role in ensuring the quality, compliance, and integrity of Acadia's clinical and commercial products. Serve as the primary quality interface with CMOs to ensure compliance with SOPs, Quality Agreements, and regulatory expectations. Minimum