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Associate Baylor Phlebotomy Jobs (NOW HIRING)

Associate Baylor Phlebotomy information

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$13

$19

$31

How much do associate baylor phlebotomy jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for associate baylor phlebotomy in the United States is $20.00, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $20.43 per hour, depending on experience, location, and employer.
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Infographic showing various Associate Baylor Phlebotomy job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $41,591 per year, or $20 per hour.

Full-time

Medical, Retirement, PTO

Posted 19 days ago


Baylor Scott & White Health rating

7.4

Company rating: 7.4 out of 10

Based on 761 frontline employees who took The Breakroom Quiz

268th of 887 rated healthcare providers


Job description

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 Research Enrollment Analyst, under general supervision, is accountable for enrolling participants in research projects, and developing and working on a self-directed research project that furthers the goals of the Investigators and Research Department.

Essential Functions of the Role

  • Coordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. May assist in complex studies with direction but does not have overall responsibility for these studies.
  • Communicates with research participants via phone calls, mail-outs, and Internet to maintain the highest level of research participant retention possible.
  • Maintains relationships with targeted research communities and investigators, patients, clinical managers, and supervisors.
  • Screens potential research participants by reviewing inclusion and exclusion criteria.
  • Enters new research participants in database and updates existing databases. Obtains and maintains consent forms. Documents the informed consent process.
  • Ensures compliance with the internal policies and procedures, and standards of JCAHO, federal, state and local governments. Submits documentation to the Institutional Review Board (IRB) autonomously and follows the process to ensure approval.
  • Attends research meetings, reads assigned literature, and makes presentations on projects at the request of the Principal Investigator (PI).
  • Works with PIs to initiate research projects. Partners with the PI to establish and implement data collection procedures and protocols and assists with the preparation of documentation to ensure compliance with regulations and submissions required for current research projects. Assists in maintaining regulatory binders.
  • Assists research physicians with study proposal development and helps to ensure that appropriate billing and charging mechanisms are in place for research charges.
  • Assists research staff to ensure that applicable study supplies are received prior to study initiation and throughout the study period.
  • Reviews data for completion and quality control and prepares data for further investigation. Works with biostatistical team as needed to create projects.

Key Success Factors

  • Phlebotomy experience required and phlebotomy certification is preferred
  • Biospecimen (e.g. urine, blood, stool, tissue) handling experience preferred
  • Experience with Epic EMR, REDCap Database and/or Verily CTMS is preferred
  • Enjoys predictable, process-oriented work and can maintain focus and quality when performing repetitive tasks
  • Ability to independently troubleshoot routine challenges, resolve issues, and identify process improvements
  • Proven written and oral communication skills
  • Excellent computer skills, including Microsoft Office, Excel, and PowerPoint
  • Ability to establish and maintain effective working relationships.
  • Ability to manage time reactive projects in order to meet deadlines
  • Ability to effectively and efficiently perform data entries in large patient databases.

Belonging Statement

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

QUALIFICATIONS

  • EDUCATION - Associate's or 2 years of work experience above the minimum qualification
  • EXPERIENCE - Less than 1 Year of Experience

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