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The Clinical Trial Assistant is to perform all duties related to the timely processing of essential clinical trial documents. • Perform system administration activities required to activate/initiate/closeout study sites or studies in Phase II to V clinical trials and manage the input of data into specific applications. • Perform manual data entry in: CTMS, TMF, CRF Imaging and various departmental databases • Ensure consistent receipt, analysis, classification, registration and disposition/filing/retrieval of hardcopy and electronic clinical trial essential docu...
Tags for this job: regulatory document clinical
ClinForce is currently seeking a GCP QA Auditor for the Cincinnati, OH area. Responsibilities will include: --Coordinate, conduct, track, and resolve Sponsor audits, Regulatory Authority inspections, investigative site audits, system audits, vendor audits, and Fraud and For Cause investigations on company- wide basis --Track, and resolve Standard Operating Procedure (SOP) deviations --Coordinate, conduct, and track regulatory training (i.e., International Conference on Harmonisation [ICH]/Good Clinical Practice [GCP], Good Laboratory Practice [GLP], and Medical ...
Tags for this job: Audit, quality assurance, GCP
Clinforce is looking for a RCRA with 4 plus years experience. Candidate must have worked in Oncology and/or Transplant. Bachelors or RN ideal. Please call or email me at firstname.lastname@example.org or 919-433-3858
Tags for this job: CRA
Clinforce is seeking a In-house CRA II based in Seattle, WA. Must have a BS and at least two years of monitoring experience. CRA II will assist Study Manager with duties pertaining to the management of clinical trials. Duties shall include, but not be limited to: the preparation of clinical documentation, source documents, CRF documents and conduct qualification visits of clinical sites, monitoring visits, close out visits, and audits of clinical sites as determined by Clinical Operations. Travel less than 20%
Tags for this job: CRA, Clinical Research Associate
Clinforce seeks a Clinical Data Manager in Seattle, WA. The candidate should have a Bachelors and 4-7 years of experience as a CDM working in a Pharma, Device or CRO setting. Duties: Assist with the clinical data process from initiation to study closure and archiving procedures (such as data management activities related to study conduct, study completion, and archiving of study materials). Develop CRFs/EDC for data collection and management, and data management plans for pre and post-market studies. Coordinate and maintain the clinical database for data con...
Tags for this job: CDM, Clinical Data Manager