System One
Job Title: Clinical Research Coordinator
Location: Dallas, TX, 75230
Schedule: Monday-Friday
Type: Contract
A leading healthcare research organization is seeking a Clinical Research Coordinator to support a Clinical Research Trial at a Dallas/Medical City location. This is a study requiring strong patient-facing skills, organizational abilities, and project management experience. If you have a background in clinical research, a minimum of a Bachelor's degree, and enjoy patient interaction, this is an excellent opportunity to contribute to impactful maternal health research. Apply today for immediate consideration.
Responsibilities
Coordinate day-to-day research operations for the PREPARE trial.
Travel between two hospital sites (Tomball and Conroe) as required.
Screen, consent, and enroll patients into the study.
Serve as a liaison between investigators, sponsors, and site staff.
Ensure protocol compliance and patient safety through accurate informed consent.
Collect, review, and enter study data into electronic case report forms (EDC).
Track and report adverse events, deviations, and study progress.
Maintain study documentation and create source tools as needed.
Support clinical procedures, such as ECGs, phlebotomy, and specimen processing/shipping.
Participate in sponsor meetings, monitoring visits, and site audits.
Requirements
Bachelor's degree required.
1+ years of clinical research experience (any therapeutic area).
Prior patient-facing role with informed consent experience.
Experience with research project management or high-volume study enrollment.
Strong organizational, communication, and time management skills.
Phlebotomy or specimen-handling experience preferred.
Certified Clinical Research Coordinator (CCRC) credential a plus.
Ref: #568-Clinical
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
Location: Dallas, TX, 75230
Schedule: Monday-Friday
Type: Contract
A leading healthcare research organization is seeking a Clinical Research Coordinator to support a Clinical Research Trial at a Dallas/Medical City location. This is a study requiring strong patient-facing skills, organizational abilities, and project management experience. If you have a background in clinical research, a minimum of a Bachelor's degree, and enjoy patient interaction, this is an excellent opportunity to contribute to impactful maternal health research. Apply today for immediate consideration.
Responsibilities
Coordinate day-to-day research operations for the PREPARE trial.
Travel between two hospital sites (Tomball and Conroe) as required.
Screen, consent, and enroll patients into the study.
Serve as a liaison between investigators, sponsors, and site staff.
Ensure protocol compliance and patient safety through accurate informed consent.
Collect, review, and enter study data into electronic case report forms (EDC).
Track and report adverse events, deviations, and study progress.
Maintain study documentation and create source tools as needed.
Support clinical procedures, such as ECGs, phlebotomy, and specimen processing/shipping.
Participate in sponsor meetings, monitoring visits, and site audits.
Requirements
Bachelor's degree required.
1+ years of clinical research experience (any therapeutic area).
Prior patient-facing role with informed consent experience.
Experience with research project management or high-volume study enrollment.
Strong organizational, communication, and time management skills.
Phlebotomy or specimen-handling experience preferred.
Certified Clinical Research Coordinator (CCRC) credential a plus.
Ref: #568-Clinical
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.