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This position will start as a Sub-Investigator but will blossom eventually into a Clinical Research Principal Investigator. Manages and reviews IVRS, CRF/EDC, if applicable. Great opportunity to get into clinical research for the first time or continue a career with an organization 100% focused on bettering the clinical trial process.
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Summary: The Clinical Research Coordinator, under the direction of the Director, CRORA and Dr. Terry Heiman-Patterson, will be responsible for the planning, implementation, and execution of Clinical Research studies in the Neurodegenerative Disease Center within the Neurology Department in the Lewis Katz School of Medicine at Temple University.
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Employ product management mindset in order to ensure the successful delivery of Clinical Research products such as Clinical Research Management Systems, Clinical Trials Management Systems, EDC (Electronic Data Capturing), eConsent, Regulatory eBinders, etc.
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Pharmasite, a Headlands Research site is looking for a Clinical Research Assistant who is a Certified Medical Assistant to assist coordinators in conducting clinical research study visits.
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Develop and deploy case report forms; including automated edit checks and indications of critical variables using EDC/CTMS. Produce and maintain database queries using MSSQL and electronic data capture tools to assure quality interim and final reporting of clinical data.
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Enforces processes for effective data management in an electronic database (EDC), electronic trial master files (eTMF), electronic patient-reported outcomes (ePRO), and Clinical Trial Management System (CTMS) Provide advice and solutions to issues to improve efficiency.
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Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed. Liaises with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables.
$80,000 - $120,000ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Clinic Research Coordinator II The Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor.
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Clinical trial database experience is required - Exp./Familiar with EDC, Medidata, RedCap or Inform is a plus but not required - Fully vaccinated with booster REQUIRED Responsibilities: - Identify and initiate communications with sites to obtain all relevant documents for project/trial.
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Proficient in Veeva eTMF and Medidata EDC. The Sr. Clinical Research Associate (Sr. CRA) provides support to Study Lead(s) in clinical study planning, execution and management. Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI and San Diego, CA. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
$120,000 - $140,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Perform data review via listings and EDC system, issue and resolve queries. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.
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Clinical Research Coordinator III A CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor.
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Experience with EDC (Electronic Data Capture) systems and software testing in a clinical research or clinical data management environment. Bachelor's Degree in related field, 8 years' experience of previous related experience in clinical research including clinical data management.
$120,000 - $170,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Employ experience with clinical database design, data loading, & database modeling concepts such as SAS, SQL, CDASH, SDTM, Medidata RAVE, Python, & Veeva EDC. Qualifications Must possess a Bachelor’s degree or foreign academic equivalent in Computer Science, Information Technology, Electronic Engineering or other technical field plus 5 years of related work experience in clinical research, project management, or similar industrial background.
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Complete source data verification of clinical study data entered in an Electronic Data Capture (EDC) system or on a case report form at sites to ensure regulatory and protocol compliance and overall accuracy.
$55 - $64.29 an hourRemoteExpandApply NowActive JobUpdated Today
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