- Merck & Co. (Rahway, NJ)
- …operational/executional arms within the business.-- - - Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM) designs strategic ... analyses , and/or develops mitigation strategies for review with clinical partners and senior leaders.- - Works... Clinical Finished Goods).- - Responsible for authoring clinical supply documentation in support of labeling… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …(FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine ... US and abroad, governmental, academic, community and industry organizations.The Senior Clinical Study Manager role...for Operational Study Strategy. This position may require the Sr . CSM to take the role of both operational… more
- Merck & Co. (Rahway, NJ)
- …teams and the operational/executional arms within the business.-- - - The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary ... cost estimates requested by Product Development Teams . - Responsible for authoring clinical supply documentation in support of labeling and packaging activities… more
- Stanford Health Care (Pleasanton, CA)
- …departmental and organizational levels. Leads and coordinates team efforts in clinical documentation integrity programs and outcomes optimization, relationship ... and long-term resolutions. + **Program Development:** + Coordinates the development of clinical documentation programs to improve the accuracy of … more
- MicroVention, Inc. (Aliso Viejo, CA)
- **12521BR** **Title:** Sr . Manager , Clinical Data Management **Job Description:** The Senior Manager , CDM oversees clinical data management ... 6. Able to work independently, as well as part of a team. **External-Facing Title:** Sr . Manager , Clinical Data Management **Posting Country:** US - United… more
- Abeona (Cleveland, OH)
- JOB TITLE Sr . Manager , Clinical / Non- Clinical Quality Department Quality Assurance Reports To Associate Director of Quality Assurance or above Ladder ... Level 5 DESCRIPTION Position Overview The Sr . Manager , Clinical / Non-...responses to external regulatory inspections. + Review and approve clinical trial protocols and associated documentation (including,… more
- BioFire Diagnostics, LLC. (Salt Lake City, UT)
- …outcomes through innovative diagnostic solutions. . We are seeking a highly skilled and motivated Sr Clinical Trial Manager to join our team and lead ... Description: We are seeking an experienced and highly motivated Senior Clinical Trial Manager to...Writes final study reports and contributes to regulatory submission documentation Key Skills and Qualifications: + Bachelor's degree in… more
- Merck (West Point, PA)
- …the operational/executional arms within the business. Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs strategic and ... prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders. + Works... Clinical Finished Goods). + Responsible for authoring clinical supply documentation in support of labeling… more
- UPMC (Mechanicsburg, PA)
- …expert clinical practice, teaching/development, and/or evidence based practice. This senior role leads the unit through difficult and complex EBP, process ... If so, then this position is for you! The Sr . Clinician is a highly developed role model of...under the direction of the Unit Director or Department Manager , assists in the completion of employee evaluations, selection… more
- Astellas Pharma (Northbrook, IL)
- …Candidates interested in remote work are encouraged to apply. **Purpose and Scope:** A Clinical Site Manager II (CSM II) serves as the primary contact point ... guidelines from study start-up through to site closure. The Clinical Site Manager will manage the site/sponsor...for trial conduct. + Ensure source and other site documentation is adequate and in compliance with ALCOA-CCEA +… more
