- 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
- 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
- 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 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
- 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
- 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
