On-Site Pediatric Clinical Research Assistant

Tekton Research; San Antonio (TX); On-site; USD 42,000 - 62,000; Full time

Job summary

Tekton Research is seeking a Clinical Research Assistant to support our pediatric clinical trials on-site. The role combines clinical tasks with study coordination, data support, and patient interaction in a fast-paced environment.

Responsibilities include patient pre-screening, phlebotomy, source documentation, and EDC data entry. On-site only, with a focus on accuracy, communication, and compliance with SOPs.

Qualifications

• 6+ months of experience as a Medical Assistant, EMT, or in a related healthcare role preferred.
• Phlebotomy experience required or strongly preferred.
• Strong attention to detail and organizational skills.
• Ability to work independently and as part of a team.
• Clinical research experience is a plus.

Responsibilities

• Support patient recruitment through pre-screening and scheduling
• Prepare source documentation and visit binders for study visits
• Request and manage medical records as needed
• Ensure completion of e-diaries by study participants
• Check patients in and out for study visits
• Coordinate participant compensation
• Answer and route incoming calls professionally
• Maintain inventory of lab and study supplies
• Perform phlebotomy (blood draws) and specimen processing
• Obtain vital signs and perform EKGs/ECGs
• Maintain accurate study documentation and master logs (ICF, enrollment, patient IDs, etc.)
• Enter data into EDC systems and resolve queries within 24 hours
• Maintain daily temperature logs and regulatory documentation
• Record adverse events and assist with sponsor reporting requirements
• Support additional clinical and administrative duties as assigned

Skills

Medical support

Phlebotomy

Attention to detail

Team collaboration

Clinical research awareness

Education

High School Diploma or GED

Some college or healthcare-related coursework

Job description

Tekton Research is seeking a Clinical Research Assistant to support our pediatric clinical trials on-site. The role combines clinical tasks with study coordination, data support, and patient interaction in a fast-paced environment.

Responsibilities include patient pre-screening, phlebotomy, source documentation, and EDC data entry. On-site only, with a focus on accuracy, communication, and compliance with SOPs.