eTeam
Job Title:
Active_Research Assistant 2
Location:
Salt Lake City, 84117
Duration:
6 Months
Pay Rate:
$35.00 - $38.68 per hour (W2)
Hours:
24 hours/week, 9:00 AM to 5:00 PM (days TBD)
Summary
Performs administrative tasks to support clinical trials
Assists with clinical procedures to collect data from patients enrolled or seeking enrollment in clinical studies
Responsibilities
Verify and correct research study information on source documents
Research data queries and variances and provide feedback to site data collectors
Enter research study data into Electronic Data Capture (EDC) systems with accuracy and quality control
Prepare, maintain, and organize research study files
Compile, collate, and submit study documentation within established deadlines
Assist in maintaining regulatory documentation
Schedule subject visits and prepare required reports and documents prior to visits
Enter visit data into Clinical Trial Management System (CTMS) to track patient visits and procedures against study budgets
Process laboratory specimens, including labeling vials and completing requisitions for storage or shipment per protocol and regulations
Package and ship specimens according to study and shipment guidelines
Perform administrative support tasks such as reception duties, office organization, and supply management
Skills
Basic knowledge of clinical trials
In-depth understanding of departmental, protocol, and study-specific procedures
Knowledge of consent forms and study schedules
Basic knowledge of medical terminology
Proficiency in MS Windows and Microsoft Office (Access, Outlook, Excel, Word)
Strong interpersonal and communication skills
Education / Experience
BS/BA in life sciences or equivalent education
Relevant work experience in a clinical or medical setting (preferred)
Examples: Clinical Research Coordinator, Nurse, Medical Assistant
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Active_Research Assistant 2
Location:
Salt Lake City, 84117
Duration:
6 Months
Pay Rate:
$35.00 - $38.68 per hour (W2)
Hours:
24 hours/week, 9:00 AM to 5:00 PM (days TBD)
Summary
Performs administrative tasks to support clinical trials
Assists with clinical procedures to collect data from patients enrolled or seeking enrollment in clinical studies
Responsibilities
Verify and correct research study information on source documents
Research data queries and variances and provide feedback to site data collectors
Enter research study data into Electronic Data Capture (EDC) systems with accuracy and quality control
Prepare, maintain, and organize research study files
Compile, collate, and submit study documentation within established deadlines
Assist in maintaining regulatory documentation
Schedule subject visits and prepare required reports and documents prior to visits
Enter visit data into Clinical Trial Management System (CTMS) to track patient visits and procedures against study budgets
Process laboratory specimens, including labeling vials and completing requisitions for storage or shipment per protocol and regulations
Package and ship specimens according to study and shipment guidelines
Perform administrative support tasks such as reception duties, office organization, and supply management
Skills
Basic knowledge of clinical trials
In-depth understanding of departmental, protocol, and study-specific procedures
Knowledge of consent forms and study schedules
Basic knowledge of medical terminology
Proficiency in MS Windows and Microsoft Office (Access, Outlook, Excel, Word)
Strong interpersonal and communication skills
Education / Experience
BS/BA in life sciences or equivalent education
Relevant work experience in a clinical or medical setting (preferred)
Examples: Clinical Research Coordinator, Nurse, Medical Assistant
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