Clinical Research Data Assistant/Pharmacy Tech

The Clinical Research Data Assistant provides administrative, data management, and study support services for clinical research studies. This position is responsible for sponsor system data entry, study reporting, document management, regulatory support, and research communications.

The Clinical Research Data Assistant works closely with Clinical Research Coordinators, investigators, sponsors, and the regulatory team to ensure accurate, timely, and compliant study documentation and reporting.

· Enter study data into sponsor electronic data capture (EDC) systems.

· Transcribe source documentation into sponsor systems accurately and timely.

· Review entered data for completeness and accuracy.

· Resolve basic data discrepancies and escalate complex issues.

· Maintain study tracking logs and databases.

Sponsor Systems Management

· Maintain user access and system tracking documentation.

· Upload required documents into sponsor portals.

· Monitor sponsor system notifications and alerts.

· Support completion of sponsor-required documentation.

· Prepare routine reports on screening, enrollment, randomization, and retention metrics.

· Track recruitment and enrollment performance.

· Maintain study enrollment dashboards and tracking tools.

· Generate reports for site leadership and study teams.

· Route study documents for review and signature.

· Assist with collection of regulatory documents.

· Maintain electronic and paper study files.

· Support regulatory filing activities.

· Assist with investigator and staff training documentation.

· Manage study email inboxes.

· Route sponsor communications to appropriate team members.

· Track action items from sponsor correspondence.

· Assist with scheduling sponsor meetings and study-related calls.

· Provide administrative support to Clinical Research Coordinators and investigators.

· Assist with study start-up documentation.

· Support study close-out activities.

· Assist with preparation for sponsor monitoring visits, audits, and inspections.

· Maintain confidentiality of participant information.

· Ensure data accuracy and completeness.

· Follow Good Clinical Practice (GCP), sponsor requirements, and site SOPs.

· Participate in quality improvement initiatives.

· Ability to perform prolonged computer-based work.

· Ability to review detailed documentation for extended periods.

· Ability to occasionally lift and move files or supplies up to 15 pounds.

· High School Diploma required.

· Associate's degree or Bachelor's degree preferred.

· Exceptional attention to detail.

· Strong data entry and computer skills.

· Strong written and verbal communication skills.

· Ability to manage multiple deadlines.

· Strong organizational skills.

· Proficiency in Microsoft Office applications, particularly Excel.

· Ability to learn sponsor systems, CTMS, eSource, and eRegulatory platforms.