Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Cognitive Research Corporation

Clinical Trial Assistant - St. Petersburg, FL

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
46
out of 100
Average of individual scores

Were these scores useful?

Job Description

Clinical Trial Assistant - St. Petersburg, FL Cognitive Research Corporation - 3.5 Saint Petersburg, FL Job Details 16 hours ago Qualifications Project coordination Full Job Description The Clinical Trial Assistant position reports to the CTA Manager. CTAs provide general logistical support for clinical trials, such as preparing meeting agendas and minutes, assisting with preparation of study site supplies and correspondence and maintenance of the Trial Master File. Essential Duties and Responsibilities Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instruction. Assists Clinical Monitoring staff with site management activities, including serving as a project team liaison for sites on assigned studies, and communicating with sites as directed. Creates and assists with maintenance of Trial Master File (TMF) and project files, including participation in file audits. Prepares and maintains site manuals, reference tools and other documents. Maintains, updates, and inputs clinical tracking information into relevant CRC systems. Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client. Manages shared mailbox, processes site requests and routes correspondence appropriately. Coordinates the ordering, packaging, shipping, and tracking of site supplies and materials. Assists with coordination of team meetings, attends meetings, and prepares agenda, meeting minutes, and action items. Perform other duties as assigned. Qualifications Bachelor's degree or RN in a related field or equivalent combination of education, training and experience. Minimum 2 years' experience in clinical research, academic, hospital or similar setting preferred. Ability to work independently with minimal supervision. Strong organizational skills. Proficiency in Microsoft Office and Adobe. Excellent verbal and written communication skills. Strong attention to detail. Ability to travel up to

Benefits

  • Dental Insurance