Will “Clinical Trial Coordinator” be Replaced By Robots? 🤔
Unknown Chance of Automation
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Job Description
Plan, direct, or coordinate clinical research projects. Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. May evaluate and analyze clinical data.
Job Details
- The SOC (Standard Occupational Classification) code is 11-9121.01
☝️ Information based on the reference occupation “Clinical Research Coordinators”.
Also Known As…
- Clinical Research Coordinators
- Research Coordinator
- Clinical Trial Manager
- Clinical Research Nurse Coordinator
- Clinical Research Manager
- Clinical Research Coordinator
- Clinical Research Associate (CRA)
- Clinical Research Administrator
- Clinical Program Manager
- Clinical Program Coordinator
- Research Associate
- Regulatory Coordinator
- Development Coordinator
- Development Associate
- Clinical Trials Specialist
- Clinical Trials Manager
- Clinical Trial Coordinator
- Clinical Trial Associate
- Clinical Support Specialist
- Clinical Study Manager
- Clinical Researcher
- Clinical Research Specialist
- Clinical Research Monitor
- Clinical Research Director
- Clinical Research Assistant
- Clinical Project Manager
- Clinical Operations Specialist
- Clinical Manager
- Clinical Data Coordinator
Tasks for “Clinical Trial Coordinator”
- Register protocol patients with appropriate statistical centers as required.
- Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.
- Arrange for research study sites and determine staff or equipment availability.
- Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
- Participate in the development of study protocols including guidelines for administration or data collection procedures.
- Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses.
- Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
- Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
- Direct the requisition, collection, labeling, storage, or shipment of specimens.
- Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
- Communicate with laboratories or investigators regarding laboratory findings.
- Participate in preparation and management of research budgets and monetary disbursements.
- Code, evaluate, or interpret collected study data.
- Organize space for study equipment and supplies.
- Contact outside health care providers and communicate with subjects to obtain follow-up information.
- Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
- Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.
- Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
- Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
- Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions.
- Solicit industry-sponsored trials through contacts and professional organizations.
- Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
- Inform patients or caregivers about study aspects and outcomes to be expected.
- Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.
- Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
- Confer with health care professionals to determine the best recruitment practices for studies.
- Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
- Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
- Develop advertising and other informational materials to be used in subject recruitment.
- Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.
- Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
- Order drugs or devices necessary for study completion.
- Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks.
Related Technology & Tools
- Digital video equipment
- Photocopiers
- Laser facsimile machines
- Personal computers
- Smartphones
- Laptop computers
- 5AM Glassbox Translational Research
- Patient tracking software
- Scheduling software
- Drug coding software
- Budgeting software
- ClearTrial
- Clinical data management system CDMS
- SAS
- TOPAZ Enterprise Software Suite
- Web browser software
- SyMetric Sciences SyMetric
- KIKA Veracity
- PercipEnz Technologies OnCore-Clinical Research Management OnCore-CRM
- Online data collection systems
- InforSense InforSense
- Microsoft Office
- FileMaker Pro
- DZS Software Solutions ClinPlus
- Microsoft Excel
- Electronic data capture EDC software
- Oracle Clinical
- Microsoft Word
- The MathWorks MATLAB
- Sierra Scientific Software CRIS
- Microsoft Project
- ePharmaSolutions eMVR
- OpenClinica
- PPD Patient Profiles
- SPSS
- StataCorp Stata
- InferMed MACRO Electronic Data Capture
- Microsoft Access
- PPD eLoader
- Qualitative analysis software
- Microsoft Outlook
- Project management software
- Phase Forward InForm GTM
- Microsoft PowerPoint
- Invivo Data EPX ePRO Management System
- StudyManager Sponsor Edition