Clinical Trial Associate Jobs in Florida

Job Description: Clinical Trials Assistant (CTA)

Qualifications

• Awareness of knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines preferred
• Knowledge of applicable protocol requirements relevant to IRB / IEC submissions
• Computer skills including proficiency in use of Microsoft Word, Excel, Publisher and PowerPoint
• Strong written and verbal communication skills including good command of English language
• Effective time management and organizational skills
• Attention to detail and accuracy in work
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
• BS/BA required; relevant experience may be considered

General Responsibilities:

• Responsible for assisting and providing support to the members of the clinical research operations project team (i.e. Clinical Project Managers, Directors, or CRAs), in order to facilitate the management of pre- and post-approval clinical trial processes including planning and execution of in-house or outsourced clinical trials.
• Provide support to clinical research operations team with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
• Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files / binders for accuracy and completeness.
• Assist clinical team with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• The CTA assists in supporting the conduct of trials and may be responsible for managing specific study and operational tasks.
• The CTA performs work within established protocols under general supervision.
• Facilitate CDA & Contract Execution Process (Routing and tracking of study specific contracts)
• Collaborate with clinical research operations team, IRB and sites to assure all required study start up documentation is accurate and submitted in a timely manner.
• Participate in creation and distribution of sponsor specific study aides/materials and communications. This includes assistance in the laboratory when needed.
• Collate documents required for the EC/IRB/HA submissions
• Initiate and maintain site and subject access within Electronic Data Capture system studies.
• OTHER DUTIES AS ASSIGNED'

Job Type: Full-time

Pay: $40,000.00 - $50,000.00 per year

Benefits:

• 401(k) matching
• Health insurance
• Paid time off
• Parental leave

Work Location: In person