- Merck & Co. (Rahway, NJ)
- …program cost estimates requested by Product Development Teams. Responsible for authoring clinical supply documentation in support of labeling and packaging ... approach to identify process inefficiencies, develop solutions, and drive continuous improvement initiatives within the clinical supply planning function. Proven… more
- Merck & Co. (Rahway, NJ)
- …enables gain of critical internal experience during scale-up of clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training ... operations, process development activities, compliance investigations/change management, authoring of GMP documentation , and lead other staff in the pilot plant as… more
- Formation Bio (New York, NY)
- …policies for upfront license revenue recognition, and milestone treatment Partners with Director of Accounting, R&D, FP&A, and clinical operations to ensure ... 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: The Director of Data Management (DM) Reporting provides leadership in Data Management ... and external stakeholders to oversee the development and delivery of clinical data programming, reporting, data visualizations, external data acquisition 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 ... for a living. Are you ready to make a difference? The Position The Director Medical Review oversees a team of Medical Reviewers responsible for Medical Assessment of… 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 ... and Compliance, Global Safety, and centralized teams (eg, Training and Documentation , Quality, Supplier and Contract Management and Digital Enablement). This role… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Key Quality Indicators (KQIs). Identify and drive initiatives for continuous quality improvement .Deputize for the Sr. Director , Medical Affairs QA as needed. ... centered around rare diseases and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director of Medical Affairs QA is… more
- Insmed Incorporated (San Diego, CA)
- …and for the future of science, we're in. Are you?About the Role:The Associate Director , EDC Programming will lead and oversee EDC programming, and database build for ... in-house clinical trials. This role will be responsible for the...audits and inspections by providing technical expertise and system documentation .Ensure data integrity, system reliability, and regulatory compliance across… more
- CoxHealth (Lake Spring, MO)
- …to work with others and communicate effectively ▪ Ability to build presentations/present Clinical Documentation Improvement to providers fluently ▪ Ability ... to work with others and communicate effectively ▪ Ability to build presentations/present Clinical Documentation Improvement to providers fluently ▪ Ability… more
- Insmed Incorporated (NJ)
- …and for the future of science, we're in. Are you?About the Role:The Sr. Director CMC QA will lead QA CMC oversight for drug products, biologics, and combination ... and internal standards.Serve as the Quality lead for GMP activities supporting clinical trial materials, including DS/DP used in early and late-phase studies.Oversee… more
- Insmed Incorporated (Minneapolis, MN)
- …the future of science, we're in. Are you?About the Role:The Associate Director Medical Science Liaison will develop and maintain professional relationships with ... assigned budget parametersIs accountable for the accurate and timely documentation of all activitiesIdentify Medical Experts, consultants, investigators, and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … operations, medical affairs, and regulatory affairs Maintain training assignments on clinical research documentation , regulatory requirements, Good Clinical ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...regulated environment. Relationship This job reports to the Senior Director of the GxP Compliance & Technical Operations or… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of GxP documentation to verify compliance and identify areas for improvement or corrective actions Collaborate with cross-functional teams to ensure that GxP ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...against established metrics Prepare and present regular reports on documentation compliance, audit results, and improvement initiatives… more
- Medalogix (Nashville, TN)
- …more about the merging of Forcura and Medalogix. Position Summary The Director , Clinical Operations leverages his/her extensive knowledge managing multiple ... 2025, Forcura, the intelligent workflow management company, and Medalogix, a clinical decision support company, announced that they have combined. Together, the… 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 ... with SDEA requirements. Relationships This position reports to the Associate Director , Safety Contracts & Supplier Management. This position works closely with… more
- Boost Home Health (Frisco, TX)
- …and enforce Boost HHC policies to ensure regulatory compliance and accurate clinical documentation . Engage in performance improvement initiatives and ... continuous improvement . Lead QA/PI activities to maintain and elevate clinical standards. Manage patient care assignments and oversee staff performance, stepping… more
- Executive Care (Leesburg, VA)
- …(EHC) Organization (HCO). This role ensures regulatory compliance, drives quality improvement initiatives, and provides leadership support across clinical , non- ... Reporting to the Governing body headed by the President and CEO, the Director of Operations and Administration is a pivotal leadership role responsible for… more
- CytomX Therapeutics, Inc. (South San Francisco, CA)
- …San Francisco, CA Candidate Location: Hybrid Travel Required: 5% Reports To: Sr. Director , Clinical Operations Department: Clinical Operations Position Type: ... ensure clinical study deliverables are met (ie, contribute to documentation , processes, and set-up activities to facilitate efficient working and effective… more
- Home Care Evolution (Vienna, VA)
- …and promptly report clinical changes to the RN Case Manager or Director of Nursing. Support and participate in Quality Assurance (QA) activities, including ... clinical record audits and ensuring documentation accuracy...using electronic medical record (EMR) systems. Contribute to performance improvement initiatives and agency survey readiness. Qualifications : Current,… more
- Aveanna Healthcare (Birmingham, AL)
- …plan of care, the interdisciplinary team, attending physician and Hospice Medical Director . Territory is primarily Jefferson County, AL. Schedule Monday - Friday ... Coordinates total patient/family hospice care under the supervision of the Director and with the interdisciplinary team, the attending physician, and other… more
