Will “Clinical Manager” be Replaced By Robots? 🤔

Unknown Chance of Automation

Sadly, the research paper did not provide any information about this occupation. Maybe have a look at our directory?

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…

Tasks for “Clinical Manager”

Participate in the development of study protocols including guidelines for administration or data collection procedures.
Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
Code, evaluate, or interpret collected study data.
Confer with health care professionals to determine the best recruitment practices for studies.
Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.
Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.
Register protocol patients with appropriate statistical centers as required.
Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
Solicit industry-sponsored trials through contacts and professional organizations.
Organize space for study equipment and supplies.
Order drugs or devices necessary for study completion.
Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks.
Direct the requisition, collection, labeling, storage, or shipment of specimens.
Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
Arrange for research study sites and determine staff or equipment availability.
Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses.
Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
Inform patients or caregivers about study aspects and outcomes to be expected.
Communicate with laboratories or investigators regarding laboratory findings.
Contact outside health care providers and communicate with subjects to obtain follow-up information.
Participate in preparation and management of research budgets and monetary disbursements.
Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.
Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions.
Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.
Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
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.

Related Technology & Tools

Smartphones
Personal computers
Laptop computers
Photocopiers
Laser facsimile machines
Digital video equipment

Oracle Clinical
5AM Glassbox Translational Research
Electronic data capture EDC software
Microsoft Word
Clinical data management system CDMS
Scheduling software
Project management software
SAS
StudyManager Sponsor Edition
TOPAZ Enterprise Software Suite
PPD eLoader
ClearTrial
The MathWorks MATLAB
Online data collection systems
ePharmaSolutions eMVR
Drug coding software
Microsoft Project
Sierra Scientific Software CRIS
Microsoft PowerPoint
Patient tracking software
StataCorp Stata
Budgeting software
Microsoft Outlook
FileMaker Pro
Qualitative analysis software
DZS Software Solutions ClinPlus
SyMetric Sciences SyMetric
Web browser software
InforSense InforSense
PPD Patient Profiles
PercipEnz Technologies OnCore-Clinical Research Management OnCore-CRM
OpenClinica
InferMed MACRO Electronic Data Capture
Microsoft Office
Invivo Data EPX ePRO Management System
Microsoft Excel
SPSS
KIKA Veracity
Microsoft Access
Phase Forward InForm GTM