- Abbott (Pleasanton, CA)
- …Associate), as needed. **2. Manage all aspects of study lifecycle to include site regulatory and quality:** Start Up + Nominate, approach, and complete ... + Identify, develop, and maintain sites capable of delivering start - up goals, study participation levels and required...up process and site initiation visits + Understand regulatory and legal requirements for study participation at a… more
- University of Washington (Seattle, WA)
- …Manager supervises and partners closely with teams responsible for fiscal management, regulatory affairs, trial start - up , and research coordination. Through ... FHCC financial systems, clinical systems and operations. - Experience in clinical trial start up - Prior management of multiple complex clinical trial budgets.… more
- Parexel (Richmond, VA)
- …investigators. + In some countries, as required, CRAs are accountable for study start - up and regulatory maintenance. Tasks may include Site Qualification ... the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start - up and for the duration of the study. +… more
- Parexel (Columbus, OH)
- …investigators. + In some countries, as required, SrCRAs are accountable for study start - up and regulatory maintenance. Tasks may include Site Qualification ... the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start - up and for the duration of the study. +… more
- IQVIA (Parsippany, NJ)
- Essential Functions * Assist Clinical Research Associates (CRAs) and Regulatory and Start - Up (RSU) team with accurately updating and maintaining clinical ... coworkers, managers, and clients. * Awareness of applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference… more
- University of Pennsylvania (Philadelphia, PA)
- …and processing regulatory documents for submission to the IRB, and all regulatory committees from study start - up to completion. Interact with study ... regulatory documents for submission to the IRB, and all regulatory committees from study start - up to completion. Data transfer and collection of imaging… more
- Parexel (Bismarck, ND)
- …responsible with CRA for enrollment delivery during study conduct + Partners with local Regulatory authorities and Study Start up teams to ensure timely ... for investigative sites throughout a study's lifecycle, responsible for site start - up , activation, relationship management, recruitment, and quality assurance.… more
- Dana-Farber Cancer Institute (Boston, MA)
- …party auditors. **Clinical Trial Management** + Track and manage assigned new protocol start - up packet; initiate, facilitate and monitor study start - up ... The ** Regulatory Coordinators (RC)** works under the direction of...and collaborate with clinical trial key stakeholders through the start - up process, provide regular updates and ensure… more
- Mount Sinai Health System (New York, NY)
- …personnel, assist in budget development by identifying research non-billables, and coordinate start - up meetings for new protocols. The position will report into ... **Job Description** A Regulatory Compliance Coordinator position is currently available within...timely manner; tracks new protocols through the internal study start - up committee system to approval and activation,… more
- 3M (Maplewood, MN)
- **Job Description:** **Job Title** Regulatory Compliance Engineer - Materials and Hardgoods **Collaborate with Innovative 3Mers Around the World** Choosing where to ... start and grow your career has a major impact...**The Impact You'll Make in this Role** As a Regulatory Compliance Engineer - Materials and Hardgoods you will… more