On-Site Pediatric Clinical Research & Phlebotomy Assistant

Tekton Research; Wichita (KS); On-site; USD 25,000 - 33,000; Part time

Job summary

Tekton Research in Wichita, KS is seeking a Pediatric Phlebotomist & Clinical Research Assistant to support our clinical trials. The role combines direct patient interaction, study coordination, and data support in a fast-paced, on-site environment.

The ideal candidate has 6+ months healthcare experience, phlebotomy skills, and strong attention to detail, with the ability to work independently or as part of a team while adhering to regulatory standards.

Qualifications

• Attention to detail and organizational skills are essential.
• Ability to work independently and as part of a team in a fast-paced clinical setting.
• 6+ months experience in a medical/healthcare role preferred or phlebotomy experience preferred.

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 and specimen processing.
• Obtain vital signs and perform EKGs/ECGs.
• Maintain study documentation and master logs.
• 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

Attention to detail

Organizational skills

Independent & team work

Healthcare experience (6+ months)

Education

High school diploma or GED

Some college or healthcare coursework

Job description

Tekton Research in Wichita, KS is seeking a Pediatric Phlebotomist & Clinical Research Assistant to support our clinical trials. The role combines direct patient interaction, study coordination, and data support in a fast-paced, on-site environment.

The ideal candidate has 6+ months healthcare experience, phlebotomy skills, and strong attention to detail, with the ability to work independently or as part of a team while adhering to regulatory standards.