Medical Coordinator Jobs

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Clinical Research Coordinator Fellow- K. Montgomery

UT Southwestern Medical CenterDallas, TX

About The Position

The UT Southwestern Clinical Research Coordinator Fellowship is a two-year program designed to train recent college graduates to become independent clinical research coordinators. This program provides fellows with direct experience and knowledge, strengthening essential management skills and developing a portfolio of work to prepare them for future graduate studies.

Requirements

  • Bachelor's Degree from an accredited 4-year college or university.

Nice To Haves

  • Applicants are those with a history of applying for a graduate program but who require additional clinical experience.
  • Ideal applicants are intending to apply or re-apply to a graduate program within 2-3 years of hire.

Responsibilities

  • Participates in a prespecified training program to prepare for independent functioning as a research coordinator fellow.
  • Observes clinical research management and administration to understand the daily challenges and decisions of clinical research staff.
  • Completes multiple health system and human subjects research training programs to become certified in good clinical practice, human subjects research, and HIPAA.
  • Interacts with various types of leadership and builds strong relationships with mentors and the research team.
  • Directly interacts with clinical research participants via telephone, telehealth, or in-person as required for research studies.
  • Works independently and/or as a member of a multidisciplinary team.
  • Attends regular research meetings, management meetings, and study-related or sponsor-hosted meetings.
  • Recruits, screens, enrolls, and follows subjects according to protocol guidelines, potentially assisting with the consent process.
  • Coordinates and schedules study procedures as per protocol.
  • Maintains coordinator data collection information for each study, which may include developing CRF's or data collection tools.
  • Coordinates regulatory aspects of the trial, including maintaining and developing regulatory information to comply with industry standards, University policies, FDA requirements, or other hospital policies.
  • Reviews and abstracts information from medical records to verify eligibility for trials.
  • Monitors patient safety by reviewing records and ensuring appropriate reporting per protocol and HRPP standards.
  • Conducts study procedures according to the protocol with proper training and check-offs to maintain scope of work.
  • Maintains subject-level documentation.
  • Presents research experience and completes a capstone project by the end of the second year.
  • Performs other duties as assigned.

Benefits

  • PPO medical plan, available day one at no cost for full-time employee-only coverage
  • 100% coverage for preventive healthcare-no copay
  • Paid Time Off, available day one
  • Retirement Programs through the Teacher Retirement System of Texas (TRS)
  • Paid Parental Leave Benefit
  • Wellness programs
  • Tuition Reimbursement
  • Public Service Loan Forgiveness (PSLF) Qualified Employer

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