- Eisai, Inc (Nutley, NJ)
- … pharmaceutical experience (ie, clinical development or operations, regulatory compliance ).Substantial experience in Clinical Quality /CQA conducting a ... management system. This role is responsible for Good Clinical Practice (GCP) and for assuring the compliance...Salary Transparency Language:The base salary range for the Senior Director , Clinical Quality Assurance is… more
- Eisai, Inc (Nutley, NJ)
- …environment and make a difference. If this is your profile, we want to hear from you. Director , Clinical Quality Assurance The Director , Clinical ... Clinical Practice (GCP) oversight, and for assuring the compliance of projects, products and programs with Eisai's Standard...Eisai Salary Transparency Language:The base salary range for the Director , Clinical Quality Assurance is… more
- Insmed Incorporated (San Diego, CA)
- …Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewReporting to the Executive Director of Clinical Quality Assurance, the Director ... Assurance (CQA) serves as a strategic leader managing quality and regulatory compliance related to GCPs,...regulatory compliance related to GCPs, acts as quality lead on the gene therapy clinical … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Senior Director of Clinical Operations will manage clinical operations ... the clinical operational and overall delivery and tactical execution of the clinical studies. The senior director will ensure a strong focus on competencies… 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
- Merck & Co. (Lower Gwynedd, PA)
- …our company's Springhouse Innovation Park facility in Lower Gwynedd Township, PA.-The successful Compliance Director candidate will lead a team that focuses on ... Job DescriptionThe PDMB Regulated Bioanalytics Department is seeking a Director to lead the Compliance team within the Late Development (AdVAnce) Vaccines… more
- Novo Nordisk Inc. (Boston, MA)
- …employee experience. Are you ready to make a difference? The Position This senior quality role will have overall responsibility for compliance topics within the ... the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future,...of Quality Excellence and Innovation and Site quality and compliance team members responsible for… more
- Monster (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary The Senior Director of Clinical Operations will manage clinical operations staff ... operational and overall delivery and tactical execution of the clinical studies. The senior director will ensure...clinical activities within the Development organization. Ensure a " Quality Mindset" is in place across the organization by… more
- Monster (Peoria, IL)
- … quality improvement initiatives that improve clinic function and clinical care. Responsibilities for Faculty portion of position: Provide care, diagnostic ... pulmonologist to fill a full-time position as Pediatric Cystic Fibrosis (CF) Director in the Department of Pediatrics' Pulmonology/Sleep Division. Our CF center is… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …s culture of excellence and compliance and working toward building a quality mindset with Medical Affairs.Support the Sr. Director 's Medical Affairs ... across all Medical Affairs programs. This role involves deputizing for the Sr. Director , representing the Quality organization at senior levels. The Director… more
- Insmed Incorporated (San Diego, CA)
- …be responsible for the development and implementation of EDC systems to support clinical trials, ensuring data quality , compliance , and efficiency throughout ... solutions comply with GCP, 21 CFR Part 11, and CDISC ODM StandardsData Quality & Compliance :Ensure EDC systems comply with regulatory requirements (eg, FDA,… more
- Monster (Oklahoma City, OK)
- Position Title: Director of Ambulatory Quality and Performance Department: Ambulatory Quality Job Description: Job Description General Description:The ... Director of Ambulatory Quality at OU Health will lead the strategic and...This role involves the development, implementation, and oversight of quality improvement initiatives, ensuring compliance with regulatory… more
- Merck & Co. (Rahway, NJ)
- …leader to drive pipeline impact and lead a talented group of pharmacometricians.This director will be part of a leadership team responsible for applying traditional ... continue to innovate our pharmacometrics capabilities on a continuous basis. The Director will be accountable for directing a team of pharmacometricians with diverse… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole Summary:The Executive Director , Value & Implementation (V&I) Outcomes Research position resides in the V&I organization, which includes Global ... cross-functional teams is a critical part of this role. The Executive Director has scientific and budgetary oversight for all outcomes research activities conducted… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Director of Operations as part of the Technical Operations team based in Raritan, ... NJ. Role OverviewThe Director of Operations is an exempt level position working...production of a personalized cell therapy to support both clinical and commercial requirements in either a Grade C… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Management related topics and establishes the oversight model for timely and quality delivery and regulatory compliance of outsourced activities.- Ensures ... to database release, data review and cleaning, database lock), to ensure data quality /integrity and regulatory compliance - Ensures that Data Management Plans are… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and tracking as well as instruct teams on how to properly conduct high quality clinical evaluation of signals in the appropriate tool (eg, disproportionality ... and fosters a culture that seeks to constantly enhance global regulatory compliance to meet signal evaluation timelines.Develop quality systems and procedures… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director (ED) for US Medical Affairs (USMA) understands Our Company's enterprise level strategies and leads cross-functionally with the ... for the US, including tactical execution by the field Regional Medical Scientific Director (RMSD) teams and is accountable for ensuring field teams execute on… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …the quality and timeline of vendor workoCollaborate with study clinical or medical lead and biostats to ensure availability of necessary dataoCoordinate ... research areas centered around rare diseases and immune disorders. SummaryAssociate Director , Global Medical Affairs Oncology Publications works with GMA Oncology… more
- Monster (Bernards, NJ)
- …across all Medical Affairs programs. This role involves deputizing for the Sr. Director , representing the Quality organization at senior levels. The Director ... high impact projects, fostering s culture of excellence and compliance and working toward building a quality ...quality mindset with Medical Affairs. Support the Sr. Director 's Medical Affairs Quality strategy by partnering… more
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