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