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SPECTRAFORCE · 19 hours ago

Clinical Research Assistant

Kansas City, MO

Contract

Onsite

New Grad, Entry Level

$30/hr - $30/hr

SPECTRAFORCE is a company dedicated to supporting clinical trials, and they are seeking a Clinical Research Assistant. This role involves performing administrative tasks to support clinical trials and assisting in the collection of data on patients enrolled in clinical studies.

ConsultingCRMInformation TechnologyLegal

Growth Opportunities

Hiring Manager

Avantika Kaila

Responsibilities

Verify and/or correct research study information on source documents

Research queries and variances, and provide feedback to the site data collector

Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness

Prepare and maintain research study files

Compile, collate and submit study information within established deadlines

Assist in maintenance of regulatory documentation

Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits

Input visit data into Clinical Trial Management System (CTMS) to track patient visits and procedures completed against the study budget

Processing of required lab specimens, labeling of vials, and accurately filling out requisitions for storage and/or shipment per the study protocol and packaging and shipment regulations

Perform various administrative support functions such as reception, office organization, and office supply management

Qualification

Clinical trials knowledgeEDC system proficiencyCTMS experienceMedical terminologyMS Office proficiencyInterpersonal skills

Required

Maintain study supplies, EDC entry/query resolution, visit scheduling and reminders, update study portals

Verify and/or correct research study information on source documents

Research queries and variances, and provide feedback to the site data collector

Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness

Prepare and maintain research study files

Compile, collate and submit study information within established deadlines

Assist in maintenance of regulatory documentation

Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits

Input visit data into Clinical Trial Management System (CTMS) to track patient visits and procedures completed against the study budget

Processing of required lab specimens, labeling of vials, and accurately filling out requisitions for storage and/or shipment per the study protocol and packaging and shipment regulations

Perform various administrative support functions such as reception, office organization, and office supply management

Basic knowledge of clinical trials

In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules

Basic knowledge of medical terminology

Skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word

Excellent interpersonal skills

BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting; e.g. clinical research coordinator, nurse, medical assistant