Clinical Research Asst 1 - PRN

About Us

Here at Baylor Scott & White Health we promote the well-being of all individuals, families, and communities. Baylor Scott & White is the largest not-for-profit healthcare system in Texas that empowers you to live well.

Our Core Values are:

• We serve faithfully by doing what's right with a joyful heart.
• We never settle by constantly striving for better.
• We are in it together by supporting one another and those we serve.
• We make an impact by taking initiative and delivering exceptional experience.

Benefits

Our benefits are designed to help you live well no matter where you are on your journey. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include:

• Immediate eligibility for health and welfare benefits
• 401(k) savings plan with dollar-for-dollar match up to 5%
• Tuition Reimbursement
• PTO accrual beginning Day 1

Note: Benefits may vary based upon position type and/or level.

Job Summary

The Clinical Research Assistant 1 helps the research team with clinical trials. They follow federal, state, and institutional guidelines. They perform tasks during all trial phases, from pre-study to study closure.

Essential Functions of the Role

• Assists with clinical research projects to ensure quality, safety, and financial outcomes. Maintains regulatory binders, recruits study subjects, and researches billing compliance. Performs procedures, collects data, and resolves queries.
• Performs specific technical tasks and procedures. These may include performing phlebotomies, recording test subject's vital signs, height, and weight. Collects and distributes subject diaries and questionnaires. Completes other study-specific procedures or tests as assigned. Records data.
• Assists with approved research subject recruitment, retention, and communication. Conducts telephone screens and participates in research marketing activities like health fairs. Builds and maintains department databases of potential subjects. Schedules study subject appointments, makes and receives subject telephone calls, and relays appropriate information.
• Maintains inventory of study-specific and clinical supplies. Works to ensure protocol compliance and efficient workflow. Organizes clinical work areas, counts and orders lab kits, ships materials, and checks and replaces expired items.
• Prepares Institutional Review Board materials and communications.

Key Success Factors

• Good written and oral communication skills.
• Good computer skills, including Microsoft Office. Access or other database experience preferred.
• Ability to establish and maintain effective working relationships.
• Ability to manage time reactive projects in order to meet deadlines.
• Phlebotomy skills preferred.

Belonging Statement

We believe that all people should feel welcomed, valued and supported.

QUALIFICATIONS

• EDUCATION - H.S. Diploma/GED Equivalent
• EXPERIENCE - Less than 1 Year of Experience