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