Research Assistant 2
Spectraforce
West Jordan, Utah
5 hours ago
Job Description
Job Title: Research Assistant 2
Duration: 6 months
Location: West Jordan, UT
Work Schedule : part-time: 24 hours/week- days TBD; hours 9am to 5pm
Additional Skills/Qualifications: EDC entry, query resolution, visit scheduling and reminders. Medidate Rave experience; cardiovascular trial experience
Summary:
A typical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
Responsibilities
Skills
Education/Experience
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
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 30.00/hr.
Duration: 6 months
Location: West Jordan, UT
Work Schedule : part-time: 24 hours/week- days TBD; hours 9am to 5pm
Additional Skills/Qualifications: EDC entry, query resolution, visit scheduling and reminders. Medidate Rave experience; cardiovascular trial experience
Summary:
A typical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
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 completenes
- 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
Skills
- 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
Education/Experience
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
Applicant Notices & Disclaimers
- For information on benefits, equal opportunity employment, and location-specific applicant notices, click here
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 30.00/hr.