SPECTRAFORCE · 2 hours ago
Clinical Research Assistant
Southfield, MI
Part-time
Onsite
New Grad, Entry Level
$26/hr - $26/hrSPECTRAFORCE is a company focused on supporting clinical trials, and they are seeking a Clinical Research Assistant to perform various administrative tasks in support of clinical studies. The role involves conducting patient chart reviews, supporting data entry, and assisting with regulatory documentation and patient visits.
ConsultingCRMInformation TechnologyLegal
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
Required
Ability to conduct patient chart reviews and determine eligibility based on inclusion/exclusion criteria
Ability to support data entry and query resolution
Ability to support additional administrative tasks, as needed (e.g., file and organize patient binders)
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
Preferred
M-F availability preferred; exact weekly schedule (24h/week) TBD and will be flexible to worker's schedule
Company
SPECTRAFORCE
Welcome to SPECTRAFORCE, your gateway to NEWJOBPHORIA™! Established in 2004, SPECTRAFORCE is now one of the largest and fastest growing U.S.
Founded in 2004
1001-5000 employees
Funding
Current Stage
Late StageCompany data provided by crunchbase