- University of Colorado (Aurora, CO)
- …and institutional research regulatory standards and guidelines. + Manage all regulatory aspects of study start - up and ongoing maintenance, ensuring ... **Research Services Professional ( Regulatory and Pre-Award) - Open Rank** **Description** **University of Colorado Anschutz Medical Campus** **Department:… more
- University of Miami (Miami, FL)
- … Analyst II reviews, prepares, and provides oversight for initial and subsequent regulatory submissions from study start - up through study closure as ... well as the maintenance of regulatory documents to ensure compliance with applicable requirements and...the process of study submissions (initial and amendment) and regulatory document maintenance; serves as point of contact for… more
- University of Pennsylvania (Philadelphia, PA)
- …of the initiation of Phase I-V clinical trials with a focus on required regulatory start - up approvals and associated site initiation documentation. Reporting ... Summary Temporary Employee - Non-Exempt Job Description Ophthalmology seeks a part-time Regulatory Affairs Start - Up Specialist-CC to facilitate, with minimal… more
- Arkansas Children's (Little Rock, AR)
- …leadership and stakeholders. *Provide training and guidance to study teams on start - up procedures, regulatory requirements, and institutional workflows. ... Type:** Full time **Department:** CC033020 Clinical Research Operations **Summary:** The Study Start - Up Project Manager serves as the institutional lead and… more
- IQVIA (Durham, NC)
- …Office Job Overview Under moderate supervision, executes the feasibility, site identification regulatory , start - up , and maintenance activities in accordance ... and accuracy. * Inform team members of completion of regulatory contractual. and other documents for individual sites. *...complete project specific information. * Review, track and follow up the progress, the approval and execution of required… more
- Abbott (Abbott Park, IL)
- …Site Contracts Associate), as needed. Manage all aspects of study lifecycle to include site regulatory and quality: + Start Up + Nominate, approach, and ... + 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
- Abbott (Minneapolis, MN)
- …Site Contracts Associate), as needed. Manage all aspects of study lifecycle to include site regulatory and quality: + Start Up + Nominate, approach, and ... + 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
- Vitalief (New Brunswick, NJ)
- …(for Industry, NIH, Cooperative Group, NCI and Investigator Initiated sponsored trials); Regulatory work required for start - up documents; Processes related ... work for Industry, NIH, Cooperative Group, NCI and Investigator Initiated sponsored trials; Regulatory work for start - up document; Contract review and… more
- Mount Sinai Health System (New York, NY)
- …Staff regarding specific protocols. + Manage clinical trials portfolio and assure timely regulatory start - up of protocols. + Monitor accruals and identify ... study enrollment, establishing a database of patients, protocol treatment and follow- up care for patients participating in clinical trials. + Collaborates with… more
- Dana-Farber Cancer Institute (Brookline, 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