Clinical Research Assistant

Tekton Research; McKinney (TX); On-site; USD 42,000 - 60,000; Full time

Job summary

Tekton Research in McKinney, Texas is seeking a Clinical Research Assistant to support our clinical trials team. The role combines clinical and administrative duties, including patient interaction, study coordination, and data support in a fast-paced on-site environment.

Ideal candidates have 6+ months in healthcare, phlebotomy experience, and strong organizational skills. This full-time, on-site position reports to the Site Manager and emphasizes adherence to SOPs and regulatory standards.

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.
• 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

Independent worker

Team collaboration

Clinical research experience

Organizational skills

Education

High school diploma or GED

Some college coursework

Job description

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Clinical Research Assistant

ENDO Full Time Administrative McKinney, TX, US

2 days ago Requisition ID: 1174

Clinical Research Assistant

Full-Time | Non-Exempt | On-Site Only

Reports to: Site Manager

Position Summary

We are seeking a Clinical Research Assistant to support our clinical research team in the daily operations of clinical trials. This role combines both clinical and administrative responsibilities, including direct patient interaction, study coordination, and data support. The ideal candidate is organized, patient-focused, and comfortable working in a fast-paced clinical research environment. Strong communication with the study team, Site Manager, and participants is essential. Adherence to site SOPs and regulatory standards is required at all times. This is a fully on-site position, no remote or hybrid work options are available.

Key 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

Required Skills & 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

Education

• High school diploma or GED required
• Some college or healthcare-related coursework preferred