Clinical Research Assistant

SPECTRAFORCE; Kansas City (MO); On-site; USD 41,328; Full time

Job summary

A healthcare staffing organization is seeking a Research Assistant in Kansas City, MO. This role involves supporting clinical trials by performing various administrative tasks to collect data on patients. The ideal candidate has a BS/BA in life sciences, basic knowledge of clinical trials, and proficiency in MS Office applications. Responsibilities include data entry, scheduling visits, and maintaining study documentation. The position offers a pay rate of $30.00/hr along with a contract employment type.

Qualifications

• Basic knowledge of clinical trials required.
• Experience in a clinical environment or medical setting preferred.
• Skilled in using MS Windows and Office applications.

Responsibilities

• Verify research study information on source documents.
• Input research study data into EDC system.
• Schedule subject visits and generate reports.
• Perform administrative support functions.

Skills

Knowledge of clinical trials

Use of MS Office applications

Interpersonal skills

Education

BS/BA in life sciences or equivalent

Job description

Job Details

Direct message the job poster from SPECTRAFORCE

This position's starting pay is: $30.00/hr.

ührung: 8 hrs/day and 24 hrs/week

8am to 5pm; days TBD

Additional Skills/Qualifications: Maintain study supplies, EDC entry/query resolution, visit scheduling and reminders, update study portals

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.

Responsibilitiesুভ>

• 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 verschil 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 Ηιρήσεις 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.
• For information on benefits, equal opportunity employment, and location‑specific applicant notices.

Company Commitment

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.

Seniority Level

Associate

Employment Type

Contract

Job Functionರುವ>

asyon Assistance