Clinical Research Coordinator I, Simmons Cancer Center

Responsibilities

Directly interacts with clinical research participants, as required, for the research study. Interacts via telephone, telehealth or in-person

Coordinate regulatory aspects of the trial including maintaining and developing regulatory information to comply with industry standards, University policies, FDA requirements or other hospital policies

Coordinate and schedule study procedures as per protocol. Approved study protocols which have order sets built may be pended by the non-licensed coordinator with oversight by PI

When outside of protocol, presents evidence and provides options (within scope of protocol) to PI

Screen, recruit, enroll and follow subjects according to protocol guidelines. May also assist with the consent process

Maintain and coordinate data collection information required for each study which may also include developing CRF's or data collection tools

Assist in developing and implementing research studies to include writing clinical research protocols

Conduct study procedures according to the protocol with proper training and check offs to maintain scope of work

Requires familiarity with research budgets to assist with or develop study budgets. May perform research billing activities, as needed, based on size of department (including linking patient calendars)

May review and abstract information from medical records for verification of eligibility for trials, as needed based on size of department

Monitors patient safety by reviewing records and ensuring appropriate reporting per protocol and HRPP standards

Review research study protocols to ensure feasibility

Assist in developing website or other social media for marketing/recruiting of clinical research study

Develop proficiency in the clinical trial management system, electronic medical record and other required data entry systems

Maintain subject level documentation

Duties performed may include one or more of the following core functions: a) Directly interacting with or caring for patients; b) Directly interacting with or caring for human-subjects research participants; c) Regularly maintaining, modifying, releasing or similarly affecting patient records (including patient financial records); or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records

Performs other duties as assigned

Preferred

ACRP or SOCRA certification a plus

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

Glassdoor

3.8

UT Southwestern is an academic medical center, world-renowned for its research, regarded among the best in the country for medical education and for clinical and scientific training, and nationally recognized for the quality of care its faculty provides to patients at UT Southwestern’s University Hospital & Clinics and affiliated institutions.

Dallas, Texas, USA

http://www.utsouthwestern.edu/

Late Stage

Total Funding

$25.1M

Key Investors

Advanced Research Projects Agency for Health

Texas Workforce Commision

2026-01-13

Grant· $25M

2022-07-07

Grant· $0.1M

Leadership Team

Chris Rubio

Interim Chief Executive Officer, Clements University Hospital

Dennis Pfeifer

AVP & CTO University Health System

Recent News

News-Medical.Net

Qualifications

Bachelor's Degree or higher degree in medical or science related field

1 year of clinical research experience

May consider additional years of experience or advanced degree in lieu of education or experience, respectively

ACRP or SOCRA certification a plus

Required skills

Represents the skills you have, click on the tags, Basic Life Support (BLS), CPR/AED, ACRP Certification, SOCRA Certification

Preferred skills

ACRP or SOCRA certification a plus

Experience

1+ years