- Prolink (Cincinnati, OH)
- Temporary Clinical Compliance Manager (2025-3186) job in Remote **Location:** Remote **Role Type:** Compliance **JOB SUMMARY** The Clinical Compliance ... guidance at implementation of new clients ? Support senior Clinical Compliance leadership to maintain client relationship for dedicated group of current… more
- GRAIL (Menlo Park, CA)
- …technology, and healthcare companies. For more information, please visit grail.com . Grail's Clinical Compliance department is seeking a compliance expert to ... pharmaceutical companies for companion diagnostic (CDx) tests. The Associate Director, Clinical Compliance will play a key leadership role in shaping and… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …target product profile (TPP) development, due diligence projects, and clinical -regulatory compliance . ResponsibilitiesEssential Duties and Responsibilities ... Clinical Development: Design and execute clinical trials for respiratory products, ensuring compliance with regulatory requirements.Collaborate with… more
- Eisai, Inc (Nutley, NJ)
- …and oversight of the Quality management system. This role is responsible for Good Clinical Practice (GCP) and for assuring the compliance of projects, products ... 15 or more years significant clinical pharmaceutical experience (ie, clinical development or operations, regulatory compliance ).Substantial experience in … more
- CHRISTUS Health (San Antonio, TX)
- …in the following area: unit specific orientation, skills/equipment training, clinical practice, and professional development. Evaluates effectiveness of staff ... and its impact on the quality of nursing care services. Utilizes clinical and staff development expertise to provide expert consultation to other units.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …You will coordinate and deliver comprehensive training programs that support clinical excellence, regulatory compliance , and medical affairs expertise across ... FDA, EMA, ICH-GCP, and other global regulatory requirements Coordinate mandatory compliance training for clinical research staff, including GCP certification… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Provide Quality oversight of all aspects of the cell therapy clinical manufacturing process.Support manufacturing activities for cGMP compliance through ... an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance , clinical quality, technical operations or cell therapy.Experience… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance , clinical quality, or cell therapy.Knowledge of cGMP regulations ... over the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile GMP environment. This includes supporting… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance , clinical quality, or cell therapyGxP Quality System knowledge, ... management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will… more
- Osage Nursing Center Rehabilitation & Skilled Nursing (Maize, KS)
- …standards ofcare. What You'll Do: Oversee nursing services, administration, and clinical supervision Ensure compliance with nursing care standards, policies, ... and procedures Supervise and guide nursing staff, including RNs, LPNs, CNAs, and CMAs Complete and update resident assessments and care plans as needed Communicate changes in residents' conditions with families, physicians, and staff Administer medications and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... The Position The position serves as the lead of Clinical Data Science & Evidence (CDSE) operations. In their...site and operational systems and tools to ensure governance compliance Responsible for CDSE internal and external newsletter development… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and… more
- Merck & Co. (Upper Gwynedd, PA)
- …--The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor, the Senior Director has ... primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Oncology medicines span all… more
- Merck & Co. (MA)
- …Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a ... focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development, including determination of appropriate… more
- Merck & Co. (Boston, MA)
- …Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the ... area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOur Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical ... existing and pipeline products to produce safe, effective, innovative medicine.The Clinical Director is responsible for protocol development and medical/ scientific… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …trained, following process and SOPs. The Director will ensure the Senior Director, Clinical Operations (Asset Lead) is fully informed of the overall portfolio status ... This will include providing innovative strategies to continuously improve Global Clinical Operations quality and metrics. IT will also include building and… more
- Legend Biotech USA, Inc. (Philadelphia, PA)
- …toxicology strategy from early research through IND-enabling studies and into clinical development, ensuring regulatory compliance and scientific rigor in ... myeloma.Legend Biotech is seeking Sr. Director of Toxicology as part of the Clinical Development team based in Philadelphia, PA or Somerset, NJ. Role OverviewWe are… more
- Merck & Co. (Rahway, NJ)
- … Clinical Trials Operations, Computer Science, Design, Detail-Oriented, Ethical Compliance , Ethical Standards, GLP Regulations, Good Clinical Practice (GCP), ... and/or PhD whose primary function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval of… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... Research & Development Division portfolio of clinical trials.- GCS is accountable for the planning, sourcing, labelling, packaging and delivery of clinical … more
