Create a Job Alert.

Enter your email below to save this search and receive job recommendations for similar positions.
Thank you. We'll send jobs matching these to
You already suscribed to this job alert.
No Thanks
US
What job do you want?

Create Job Alert.

Get similar jobs sent to your email

Apply to this job.
Think you're the perfect candidate?
Apply Now

You’re being taken to an external site to apply.

Enter your email below to receive job recommendations for similar positions.
Clinical Research Assistant at Ascent Services Group

Clinical Research Assistant

Ascent Services Group San Antonio, TX Contractor
$0.00 - $31.00 / hour
Apply Now

Create Job Alert.

Get similar jobs sent to your email

Clinical Research Assistant 
San Antonio, TX
Pay rate: $31.00/hour
8-Month+ Contract

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. This position will be assisting with COVID-19 related research. 

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
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
 

Recommended skills

Electronic Data Capture
Clinical Trial Management Systems
Storage (Warehousing)
Clinical Trials
Scheduling
Packaging And Labeling
Apply to this job.
Think you're the perfect candidate?
Apply Now

Help us improve CareerBuilder by providing feedback about this job: Report this job

Report this Job

Once a job has been reported, we will investigate it further. If you require a response, submit your question or concern to our Trust and Site Security Team

Job ID: 21-00200

CareerBuilder TIP

For your privacy and protection, when applying to a job online, never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. Learn more.

By applying to a job using CareerBuilder you are agreeing to comply with and be subject to the CareerBuilder Terms and Conditions for use of our website. To use our website, you must agree with the Terms and Conditions and both meet and comply with their provisions.