- ICON Clinical Research (Brentwood, TN)
- …to the Central CDP Review Team (CDPRT) and Sponsor. **What you need for Study Start Up Associate I - Regulatory Submissions** * A high school diploma or ... Study Start Up Associate ... Study Start Up Associate II - US,...regulatory and site level critical documents required for study site activation in accordance with ICON SOPs/WPs, Sponsor… more
- BeiGene (San Mateo, CA)
- …of study in countries in assigned region in close collaboration with regional study start up team and regulatory affairs. + Ensures regional and ... resolution of issues within the region for the assigned study or portfolio of studies . + Contributes... timelines. + Generates, manages, and maintains high quality study start up and recruitment timelines for… more
- System One (Basking Ridge, NJ)
- …in planning and execution of clinical studies , under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in ... Role: Clinical Study Associate I Type: 12 month...ready. Track study metrics such as site start -up, Investigator/site performance, recruitment, regulatory documents, TMF… more
- Colorado State University (Fort Collins, CO)
- … studies are conducted according to protocol and meet regulatory requirements. Percentage Of Time20 Job Duty CategoryStudy Conduct Procedures Duty/Responsibility ... Posting Detail Information Working TitleRA II - Study Lead, ARPA H Position LocationFort Collins, CO...studies are conducted according to protocol and meet regulatory requirements Percentage Of Time10 Application Details Special Instructions… more
- BeiGene (Emeryville, CA)
- …study timelines. + Manages regional leaders to generate and maintain high quality study start up and recruitment timelines for region and tracks their ... _Line management responsibilities:_ + Provides leadership, management, and/or mentorship to associate directors, clinical study managers at various levels for… more
- Battelle Memorial Institute (West Jefferson, OH)
- …and quality control (QC) in electronic data acquisition systems + Assist with study start preparation activities including requests for equipment, generating ... critical services for our clients-whether they are a multi-national corporation, a small start -up or a government agency. We recognize and appreciate the value and… more
- Dana-Farber Cancer Institute (Boston, MA)
- …. Responsibilities include coordinating cohort studies activities and related studies , providing training to research staff, regulatory submissions, and ... The RPM will be supervised and supported by the Associate Director of Cohort Studies to develop...+ Initiates, plans, facilitates and oversees the research project start -up, active and close out phases; for studies… more
- College of Lake County (Grayslake, IL)
- Adjunct Faculty, Legal Studies - Probate Law or Civil Litigation Bookmark this Posting Print Preview | Apply for this Job Posting Details Posting Detail Information ... Posting Number F01025 Position Title Adjunct Faculty, Legal Studies - Probate Law or Civil Litigation Internal Position Title Adjunct Faculty, Legal Studies -… more
- Cargill (Fort Morgan, CO)
- …around the world and connect with something greater. **Food Safety, Quality, and Regulatory Associate Position:** The purpose of this position is to develop ... if your ideas could nourish the world? As an associate , we transfer your knowledge and skills into profound...of increased complexity across the Food Safety, Quality, and Regulatory (FSQR) job family at various locations across Cargill.… more
- Community Health Network (Indianapolis, IN)
- …submit start -up regulatory packets to Sponsor and IRB + Oversee study start -up activities to including reporting and communicating with stakeholders on a ... Difference** The Research Regulatory Coordinator leads, coordinates and oversees regulatory processes across multiple studies of different therapeutic areas… more
- College of Lake County (Grayslake, IL)
- Adjunct Faculty, Spanish/Latin American Studies Bookmark this Posting Print Preview | Apply for this Job Posting Details Posting Detail Information Posting Number ... F01097 Position Title Adjunct Faculty, Spanish/Latin American Studies Internal Position Title Adjunct Faculty, Spanish Department CommArts/Hum/Fine Arts Div Position… more
- Stanford University (Stanford, CA)
- …Duties include: + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start -up through close-out. ... Clinical Research Coordinator Associate : Fixed Term - 1 Year **School of...to perform duties related to the coordination of clinical studies . Coordinate moderately complex aspects of one or more… more
- Abbott (Alameda, CA)
- …generating monitoring trip reports, and track resolution of action items. + Participate in study start up activities. + Responsible for ensuring shipment of ... but not limited to planning and implementation of clinical studies from concept to clinical study report...+ Participate in the interim and final reviews of study data in preparation of regulatory submissions.… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies . Ensure consistency within the ... An Associate Director Program Operations Leader (POL) is responsible...Reviews key metrics and Key Performance Indicators (KPIs) across studies and within clinical program(s) to track study… more
- CSL Behring (King Of Prussia, PA)
- …**Responsible for oversight of TMF, always ensuring inspection readiness** **Report main study performance information, including study start -up metrics, ... for a clinical studies and a clinical prgrams and the end-to-end study delivery of all operational activities and budget management relating to assigned clinical… more
- J&J Family of Companies (Columbus, OH)
- …, data science and new clinical and physiological applications. **Key Responsibilities:** + Study start -up and study conduct activities including drafting ... site initiation visits; train site personnel on sponsor and regulatory requirements for study conduct; participate in...studies are being carried out in accordance with study + Assess all data documentation, reports, records, transcripts,… more
- Hartford HealthCare (Bridgeport, CT)
- …efforts to initiate new studies , attending IRB meetings to expedite the start -up process. The SrCRA supervises all study activity and may delegate ... analysis and development of protocols. * Enrolls patients in studies by screening for eligibility criteria, consulting with physicians...study activity as required of a Clinical Research Associate This is an onsite position** * Bachelor degree… more
- Stanford University (Stanford, CA)
- …include:** + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start -up through close-out. ... Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Aug 22, 2024 Requisition # 104337 TheDivision… more
- Stanford University (Stanford, CA)
- …include*:** + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start -up through close-out. ... Cancer Clinical Research Coordinator Associate - Pediatric Oncology **School of Medicine, Stanford,...utilize this knowledge to support early phase clinical research studies in Pediatric Oncology. We are seeking candidates with… more
- Stanford University (Stanford, CA)
- …include:** + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start -up through close-out. ... Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States**...closely with a team. The projects involve novel research studies in the Advanced Cardiovascular Imaging Lab and the… more