- Summit Care LLC (Cheney, KS)
- …Therapist Assistant Reports to: Facility Rehab Director/Regional Director, Clinical Supervision from Physical Therapist FLSA Status: Non-Exempt Classification: ... Clinical Supervises: Students Position Summary: The Physical Therapist Assistant...to adult and geriatric patients, represents a commitment to quality of care in all interactions with patients, caregivers,… more
- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you. Director, Clinical Quality Assurance The Director, Clinical Quality Assurance position ... for design, delivery and execution of the North America (NA) Clinical Quality Assurance (CQA) strategy including audit and inspection management and oversight… more
- Neuralink (Austin, TX)
- …to establish efficient systems for compliance. Job Description and Responsibilities: As a Clinical Quality Specialist, you will conduct audits and ensure that ... activities involving effective execution of corrective action requirements Lead clinical quality process improvement initiatives Required Qualifications:… more
- Merck & Co. (Rahway, NJ)
- …organizations ( as a lead GCS Planning program representative ) such as clinical development, regulatory, quality and other supply chain areas to negotiate ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing.... - Familiarity with Good Manufacturing Practices (GMP) requirements, quality procedures, and Standard Operating Procedure (SOP) execution. -… more
- Merck & Co. (Rahway, NJ)
- …for clinical supplies . - Interacts with key partner organizations such as clinical development, regulatory, quality and other supply chain areas to address ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...(GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full c ompany's Research… more
- Blue Cross Blue Shield of Massachusetts (Boston, MA)
- …Bring your true colors to blue. The Role The Sr. Program Manager, Clinical Quality is responsible for developing, managing, coordinating, and contributing to ... activities on behalf of the organization. The Sr. Program Manager, Clinical Quality works closely and collaboratively with all HMM areas, Performance Measurement… more
- Vaxcyte (San Carlos, CA)
- …decision making. Summary: We are seeking a dedicated and experienced Senior Manager, Clinical Quality Assurance, to join our dynamic team. The ideal candidate ... skills, with a keen attention to detail. Reports to: Director, Clinical Quality Assurance Location: San Carlos, CA; Open to Remote Compensation: The… more
- Sanofi (Morristown, NJ)
- …life / medical / natural sciences or scientific discipline or equivalent Experience in Clinical Quality Assurance and/or in Clinical Trials such as ... Job Title: Clinical Project Quality Manager Location: Morristown, NJ About the Job Are you ready to shape the future of medicine? The race is on to speed up drug… more
- Merck & Co. (North Wales, PA)
- …protocol in collaboration with Data Management/Programming.Collaborating cross-functionally to monitor clinical data to ensure quality , completeness, and ... SummaryThis position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof.- In this position, you will have the… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality , or cell ... the treatment of multiple myeloma.Legend Biotech is seeking a Quality Systems Lead as part of the Quality...within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.… more
- Merck & Co. (Rahway, NJ)
- …protocol in collaboration with Data Management/Programming. Collaborating cross-functionally to monitor clinical data -to ensure quality , completeness , and ... scientific -pl anning and execution of one or more clinical trials or significant aspects thereof . In this...Job Responsibilities - Responsible for leading specific aspects of clinical /scientific execution of clinical protocol(s) . This… more
- Cedent (Boston, MA)
- Position: Clinical , Regulatory, and Quality Manager ??"?Location: Boston, MA (Onsite) What You'll Do: Lead Clinical Research, Regulatory Affairs, and ... team growth Who You Are: ? 3-5 years of experience in Clinical , Regulatory, and Quality roles within medical devices or healthtech ? Strong knowledge of FDA… more
- Merck & Co. (Rahway, NJ)
- … Clinical Trial Operations (GCTO) Regional colleagues and Global Development Quality (GDQ) to address clinical supply related topics.-Responsible and ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...(GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full Research & Development… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality , or cell ... seeking QA Validation Specialist III as part of the Quality team based in Raritan, NJ. Role OverviewThe QA...within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment.… more
- Eisai, Inc (Nutley, NJ)
- …the clinical operations function in the execution of all aspects of end-to-end clinical trials with the utmost compliance and quality consistent with Good ... clinical operations activities. These activities directly impact the timeliness, quality , and successful execution of clinical studies in accordance with… more
- Genmab (NJ)
- …of our Global Medical Writing team, you will drive the development of high- quality clinical documents to support operational, medical, and regulatory activities ... part of a dynamic, collaborative team that values innovation, quality , and scientific integrity? At Genmab, we are seeking...us tell the story of our science through compelling clinical and regulatory documents. You'll be at the heart… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …QualificationsMust have at least 7 or more years of professional experience in Quality and clinical development in the Pharmaceutical industry, with involvement ... audits assigned. Support conduct of document audits including eTMF, Clinical Study Reports and Common Technical Document submission.ResponsibilitiesSupport audit… more
- Formation Bio (New York, NY)
- …efforts to ingest and transform unstructured and structured research, biomedical and clinical data into high- quality , actionable assets that power discovery and ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …strategies and tactics that will Improve strategic planning Expand and improve the quality of clinical research Increase accuracy of medical and marketing ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to ensure appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
