- Insmed Incorporated (San Diego, CA)
- …Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewReporting to the Executive Director of Clinical Quality Assurance, the Director of ... compliance related to GCPs, acts as quality lead on the gene therapy clinical development team, and collaborates on other related activities performed by Clinical… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Executive Director , Global Clinical Development resides within the Oncology at Eisai. This Executive ... vendor management, budget planning & resource management.Demonstrated track record as Study Director (or equivalent role) with Global Clinical Lead or … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryAssociate Director , Global Medical Affairs Oncology Publications works with GMA Oncology ... activities- Oversee the quality and timeline of vendor work- Collaborate with study clinical or medical lead and biostats to ensure availability of necessary data-… more
- Genmab (NJ)
- …us!Role:The Associate Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead for both early ... responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and… more
- Merck & Co. (Durham, NC)
- …a wide range of business activities.- Reporting directly to the Director , Supply Chain Management, the successful candidate's primary responsibilities will include ... enterprise resource planning (SAP) data accuracy and transactional disciplineSupport Director in continual evaluation of the SCM organization (assess needs… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJoin Our Team as an Associate Principal Scientist/Associate Director in Biologics Drug Substance Commercialization!Are you ready to make a significant ... in and/or spearhead cross-divisional technical teams focused on late-stage clinical process development, characterization, and technology transfer of biopharmaceutical… more
- Eisai, Inc (Exton, PA)
- …If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading and building a ... new products in development through their lifecycle (Preclinical through phase III clinical development) at the Biologics Pilot Plant as well as supporting… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …project. This position prepares trainings, supports CAPA investigations, case review, documentation reviews in collaboration with the ICSR management and CRO/Vendor ... oversight groups for case processing activities and reports to the Director of PV Case Management.Responsibilities:ICSR Processing: Oversees QC activities, supports… more
- Insmed Incorporated (Los Angeles, CA)
- …Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director Medical Science Liaison will develop and maintain professional ... assigned budget parametersIs accountable for the accurate and timely documentation of all activitiesIdentify Medical Experts, consultants, investigators, and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …in? Are you ready to experiment with us? The Position The Director , Market Intelligence and Portfolio Insights will leverage Competitive Intelligence methodologies ... to provide key insights into the biopharmaceutical landscape across clinical , commercial, and enterprise domains. This role involves applying data interpretation and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …ED&AA, IT, Ethics and Compliance, Commercial, Patient Services, CMR ( Clinical , Medical, Regulatory), Finance, and Novo Nordisk global colleagues. Externally, ... Effective in fast-paced environments with a focus on quality and documentation Skilled in change management and guiding teams through transitions Communication… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Operations, including but not limited to - Commercial, Patient Services, CMR ( Clinical , Medical, Regulatory), Finance, and Novo Nordisk global colleagues, to deliver ... in fast-paced environments with a focus on quality and documentation .Skilled in change management and guiding teams through transitions.Excellent communication… more
- Merck & Co. (Rahway, NJ)
- …& Development team that designs and develops benchtop/low-volume to high-volume clinical and commercial assembly equipment and processes for medical devices/drug ... delivery systems. Reporting to the Director responsible for this area, you will partake in...semi-automated and automated equipment, conduct functional testing, assist in clinical batch manufacture as an equipment subject matter expert,… more
- Merck & Co. (Rahway, NJ)
- …Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of scientists in solving ... for successful transfer of assays. Plan assay optimization and documentation to meet program deadlines.Authoring and reviewing internal technical reports,… more
- Leica Biosystems (Miami, FL)
- …diagnostics specifically Companion Diagnostics and digital pathology in the clinical oncology environment. The Senior Principal, Regulatory Affairs will provide ... driving innovation and excellence in the Biopharma sector.This position reports to the Director , Regulatory Affairs and is part of the Global Regulatory Affairs and… more
- Tufts Medicine (Burlington, MA)
- …advisors and leaders. The Director oversees the manager and clinical documentation specialists (CDSs) in planning, implementing improvements, and ... of CDI serves as the programmatic and operational leader for Clinical Documentation . The Director works to leverage performance, provide feedback, and… more
- Rochester Regional Health (Rochester, NY)
- Job Title: Director , CDI Department: Clinical Documentation ImprovementLocation: Riedman CampusHours Per Week: 40Schedule: Monday - Friday, 8am - ... 4:30pmSUMMARY The Clinical Documentation Improvement Director provides a key role in advancing the long term success of the Clinical Documentation … more
- Elevance Health (Richmond, VA)
- ** Clinical Documentation and Claims Integrity Director ** **Location:** Alternate locations may be considered. This position will work a hybrid model (remote ... and quality of life through home-care and community based services. The ** Clinical Document Improvement Director ** is responsible for leading encounter… more
- Parkview North Hospital (Fort Wayne, IN)
- Summary Supports the Clinical Documentation Director in daily operations of the Clinical Documentation Integrity Team, and in mentoring and ... of staff. Is responsible for overseeing the efficient operation of the Clinical Documentation staff, including standard work and high-quality outcomes.… more
- LifePoint Health (Gallatin, TN)
- …and support, as well as assist with education and training related to improving clinical documentation . Reports to: Market Director of Health Information ... Facilitates improvement in the overall quality, completeness, and accuracy of clinical documentation . Through concurrent interaction with physicians, case… more
