Clinical Research Coordinator I

Clinical Research Coordinator I (103233)# Clinical Research Coordinator I (103233)Cedar Park-Medical Parkway - Cedar Park, TX 78613; Austin-Jollyville - Austin, TX 78759Start Date 06/18/2026## OverviewSalary Range$55,000.00 - $65,000.00 Salary/yearPosition TypeFull Time## Description**Job Summary:**Under the general supervision of a physician and the clinical and clinical research team in an outpatient setting, the Clinical Research Coordinator I (CRC I) is responsible for executing study-related activities from study startup through closeout. All tasks are conducted in compliance with Good Clinical Practice (GCP), ALCOA-C principles, sponsor requirements, and USDP standards. The CRC I supports the Principal Investigator in the conduct of clinical trial visits, ensuring that participants are appropriately scheduled and that all protocol-specified procedures are completed accurately and in a timely manner.**Duties and Responsibilities:*** Maintain all aspects of study protocol during recruitment, screening, enrollment, and follow-up visits* Assist the PI, and team when applicable, the informed consent process with patients and their families* Conduct and coordinate patient visits including patient demography, vitals, EKG, phlebotomy, photography, administering investigational drug, assisting PI and sub-investigators with physical exam, and scheduling appropriate follow-up visits* Communicate frequently with contract research organizations, IRB, Sponsors, Central Lab Facilities, and other outside vendors to manage the day-to-day needs for current and prospective trials* Maintain all source documents and investigational drug accountability records* Enter source data into EDC efficient and accurately* Maintain regulatory documents related to ISF* Follow SOPs, policies, and procedures as set forth by the company* Review EDC for accuracy and completion, and resolve queries as they arise* Assists with direct patient care procedures, as required by the study, including biopsies, surgeries, cosmetic procedures and related tasks* Process prescriptions and prior authorizations as directed by physician. Address patient and/or pharmacy questions concerning medication. Enroll patients in patient education/assistance programs* Ensure necessary study related documentation and correspondence study subjects, study teams, vendors, and sponsors* Scans correspondence into EMR* Practices safety, environmental, and/or infection control methods* Assist clinical research manager in delegated tasks* Performs miscellaneous job-related duties as assigned* Process blood and urine samples in accordance with IATA and OSHA standards* Prepare necessary documentation for SIV, IMV, COVs and other sponsor related meetings* Working knowledge, at minimum, of all applicable protocols. Some team members may be assigned as the primary coordinator for a specific protocol, and should therefore have in-depth knowledge of that protocol## Qualifications**Experience Requirements:*** At least 1 year of research experience, *preferred** At least 1 year of direct patientexperience, *preferred***Knowledge, Skills and Abilities Requirements:*** Meticulously detail oriented, professional attitude, reliable* Organizational skills to support accurate record-keeping* Ability to follow verbal & written instructions* Interpersonal skills to work as a team with patients and outside parties* Able to communicate effectively in English, both verbally and in writing, with proper grammar and spelling skills to avoid mistakes or misinterpretations* Mathematical and analytical ability for basic to intermediate problem solving* Basic to intermediate computer operation* Proficiency with Microsoft Excel, Word, and Outlook* Specialty knowledge of systems relating to job function* Knowledge of state and federal regulations such as ICH GCP, IATA; general understanding of HIPAA guidelines**Supervisory Responsibilities:*** This position has no supervisory responsibilities.**Benefits**:* Medical, Dental, & Vision* 401k* PTO & Paid Holidays* Company Paid Life Insurance* Employee Perks Program #J-18808-Ljbffr