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Bachelor’s degree, preferably in areas such as biological sciences, health care management or life sciences research; BSN/RN or experience with management of clinical trials. Participates in assigned activities related to user acceptance testing (UAT) of clinical systems, including EDC and interactive response technology (IRT) and may contribute to the authoring of systems requirements.
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AMCR is looking for a Research Assistant to organize the collection of data, documentation, and record-keeping activities pertaining to clinical research studies. Excellence in clinical research, accelerating access to treatments that change lives.
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The candidate will be coordinating clinical research protocols from study start up to close out. Collects, verifies, organizes and records clinical information and data in electronic data capture systems (EDC.
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Collaborate and consult with the MRDC’s technical supporting team on the technical problem troubleshooting and system upgrade and maintenance activities of the MRDC in-house’s Clinical Research Data Management System (CRDMS) and its components (e.g., Inform EDC, Central Designer, Central Coding.
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Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or equivalent Clinical research certification through SOCRA for ACRP.
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PROMETRIKA is a full-service clinical research organization (CRO) with extensive experience in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance.
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This includes responsibility for the compilation and transcription of research patient data and study-related information into case report forms (CRFs) into sponsor specific electronic data capture systems (EDC.
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On clinical research and trials in various phases and design. Participation in the protocol-specific data management database closure, project closure, and study Trial Master File archiving of all data management deliverables (e.g., subject CRFs, final query reports, final audit trial reports, interim and final raw data in Clinical Data Acquisition Standards Harmonization (CDASH), data from external sources/transfers, essential data management documents.
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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.
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Must Haves: previous experience as a Clinical Research Coordinator, Data entry experience. Part-Time Clinical Research Coordinator. This candidate will work closely with all research staff to collect, store and maintain data in accordance with FDA Regulations, International Council of Harmonization and Good Clinical Practices.
$20 - $30 an hourPart-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Research Assistant I The Research Assistant will be responsible for assisting the clinical research staff in conducting clinical research trials. KNOWLEDGE & EXPERIENCE Education: High school diploma or equivalent required Experience: Prior experience in clinical research is not required but preferred Credentials: Phlebotomist certificate preferred Medical Assistant Certification preferred Knowledge & Skills: Knowledge of medical terminology required Must be detail-oriented and demonstrate attention to detail Excellent customer service skills Excellent computer skills Powered by JazzHR.
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Accurately enters data from source documentation listed above, outside hospital records, and/or hard-copy research-specific documents, into study specific electronic data capture (EDC) systems for clinical research trials within 5 days of the patient visit EDCs include, but are not limited to, RedCap, Inform, Medidata Rave, Viva Vault, and Trial Master.
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Some key aspects of the job will be to have prior clinical research experience - this will be onsite with EDC entry query resolution QC. Review/prescreen charts from EHR prescreen media referrals visit scheduling and reminders.
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MUST HAVE EXPERIENCE WITH CLINICAL DATA SETS, EDC and non-crf data, and have strong analytical skills with the ability to work with a variety of large and complex datasets including (but not limited to) basic research datasets and clinical data.
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Required: Must have experience as a Clinical Research Coordinator (2 years+) -2 years+ of EMR and EDC experienceExperience Level:Entry LevelAbout Actalent Actalent is a global leader in engineering and sciences services and talent solutions.
$25 - $30 an hourPart-timeExpandApply NowActive JobUpdated 5 days ago
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