Job description
Job description
Urology Clinics of North Texas strives to provide highly positive medical outcomes, proven advanced technology and pharmaceuticals. We deliver care in locations convenient to patients throughout the Dallas, Collin, Rockwall, and Tarrant County areas.
Clinical Research Coordinator (CRC) comprises an integral part of the research team. Working under the PI, he/she is responsible for conducting the study in accordance with federal and hospital regulations. Some responsibilities of the Clinical Research Coordinator (CRC) depending on need include:
- Facilitate and coordinate the daily cancer clinical trial activities
- Conduct clinical trials per Good Clinical Practice and CFR guidelines
- Work directly with on-site research staff of Investigators, Nurses, Medical Assistants.
- Accurate and timely trial data collection and reporting
- Submit regulatory documents to IRB and Sponsor
- Attend investigator meeting(s)
- Obtain physician signatures
- Recruit subjects/patients
- Screen, track and schedule trial pts
- Teach subjects/patients about protocol expectations for trial visits
- Perform study/protocol procedures in a detailed, accurate manner
- Maintain study files on site
- Report all adverse events and SAEs
- Collect laboratory specimens, processing and shipping lab work
- Maintain communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel.
- Complete case report forms (CRF) and electronic data capture (EDC) for PI review and approval
- Coordinate site study monitor and sponsor visits
- Maintain study-specific supplies
- Prepare for study closure and archiving
- Knowledge of medical terminology (Oncology and Urology preferred).
- Knowledge of good clinical practice, FDA, OHRP, HIPAA policies.
- Proficiency with the Microsoft Office Suite, Google Docs, Sharepoint.
- Meticulous attention to details
Job Qualifications:
- 3 years of equivalent experience in medical clinic, research coordination required
- CCRP, ACRP certification preferred but not required
- Prior experience with Urology and Oncology clinical trials preferred
- Performs primary duties with greater independence and has progressed to performing more advanced skill sets as directed.
- Some EMR (electronic medical records) experience required
- Some Electronic Data Capture (Rave, Oracle, Inform, etc.) experience required
Knowledge, Skills & Abilities:
- Excellent organization and communications skills required.
- Strong interpersonal skills – ability to effectively interact with all levels of staff and external contacts.
- Must be detail oriented and have the ability to follow-through.
- Ability to effectively manage time and prioritize workload.
- Must practice discretion and adhere to site confidentiality guidelines at all times.
- Must have computer skills including the use of Microsoft Office.
Job Type: Full-time
Pay: From $58,000.00 per year
Benefits:
- 401(k)
- Dental insurance
- Employee assistance program
- Flexible spending account
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Retirement plan
- Vision insurance
Schedule:
- Monday to Friday
Supplemental pay types:
- Bonus pay
Ability to commute/relocate:
- Dallas, TX 75231: Reliably commute or planning to relocate before starting work (Required)
Experience:
- Clinical Research: 3 years (Preferred)
License/Certification:
- CCRP or ACRP (Preferred)
Work Location: One location
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