Texas Licensed Clinical Research Coordinator

Job Summary

Supporting Texas Oncology's Clinical Research program in a remote capacity, the Texas Licensed Clinical Research Coordinator will manage prescreening activities for clinical trials, including patient eligibility assessments and collaboration with research teams, in a full-time role.

Key responsibilities

• Conducts prescreening activities by reviewing patient records and identifying potential candidates for clinical trials based on eligibility criteria
• Maintains accurate documentation of prescreening activities, referral outcomes, and trial matching results in relevant systems
• Collaborates with physicians and research staff to communicate trial opportunities and facilitate patient referrals for further evaluation

Required qualifications

• Associate's degree in a clinical or scientific related discipline required; Bachelor's degree preferred
• Minimum one year of experience in a clinical or scientific related discipline, preferably in oncology
• For Level 2: Minimum five years of experience in a clinical or scientific related discipline required
• SoCRA or ACRP certification preferred for Level 2 and Sr roles
• For Sr Level: Minimum seven years of experience in a clinical or scientific related discipline required, with five years in oncology/research preferred