Clinical Research Coordinator
Job Description
Job Title: Clinical Research Coordinator
Location: Fort Worth, TX
Start Date: Mid-July 2026
Duration: Part-time. Open ended contract.
Schedule: M-F standard business hours. The amount of hours per week will vary based on study needs. Days on sites will vary from 3-8 hours (dictated by # of participants being treated that day (1 = ~ 3 hours; 2 = 4-6 hours; 3 = 8 hours) - Where possible (and applicable) we will always request the site to "stack" participants.
Study Type: Ophthalmology Device.
Coordinate and manage the participation of individuals in clinical trials, ensuring compliance with study protocols and regulatory requirements.Collect, organize, and maintain accurate and up-to-date clinical trial data, assisting with data entry, verification, and reporting.Support and facilitate all aspects of clinical trial activities, including scheduling appointments, communicating with participants, and collaborating with research teams.Ensure proper documentation and adherence to Good Clinical Practice (GCP) guidelines, institutional policies, and regulatory standards.Assist in resolving any issues related to participant eligibility, protocol adherence, or data discrepancies.Act as a liaison between study teams, investigators, sponsors, and participants to ensure smooth trial operations.Contribute to the development of study-related materials and provide administrative support as needed.#MedixLS
For California Applicants:
We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA).
This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.
Our commitment to our core purpose of positively impacting 20,000 lives affects not only the way we interact with our clients and talent, but also with our co-workers! The goal is lofty, but it is made attainable through the hard work and dedication of our teams and their willingness to lock arms together. Are you ready to lock arms with us?
