Work in Iowa Healthcare Jobs

Research Assistant 1

job details:

• location:West Des Moines, IA

• salary:$30 - $32 per hour

• date posted:Tuesday, February 16, 2021

• experience:1 Years

• job type:Contract

• industry:Professional, Scientific, and Technical Services

• reference:35312

job description

Research Assistant 1

job 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. The Research Assistant will be working onsite in Des Moines, IA

location: West Des Moines, Iowa

job type: Contract

salary: $30 - 32 per hour

work hours: 9 to 5

education: Bachelors

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

qualifications:

• 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

• 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

skills: Clinical research

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.