Research Coordinator (Oncology Clinical Trials)

Location: Irving, Texas, United States

Salary: $43,400–$108,200 annualized base pay

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The role is associated with NEXT Oncology, an Avacare business.

What you will do

• Coordinate screening, eligibility assessment, scheduling, and oversight of protocol-required clinical trial activities.
• Support informed consent and re-consent processes, assess patient understanding, and address barriers to effective decision-making.
• Educate patients, families, and clinical staff about study participation, procedures, and protocol-specific requirements.
• Collaborate with investigators, pharmacy, sponsors, monitors, auditors, and interdisciplinary teams to maintain protocol compliance and patient safety.
• Report adverse events, deviations, violations, and noncompliance, and contribute to corrective and preventive action plans.
• Maintain source documentation, enter and verify clinical trial data, respond to database queries, and support data quality activities.

Requirements

• Knowledge of standard research and oncology care practices.
• Typically 5 or more years of experience.
• Current Texas or Virginia Registered Nursing License for Registered Nurses.
• Bachelor’s degree required for non-RN candidates.
• Ability to manage informed consent, patient eligibility, protocol procedures, clinical documentation, and electronic data capture.

Nice to have

• Oncology clinical trial experience.
• Research coordination experience.

Culture & Benefits

• Mission-driven clinical research environment focused on collaboration, precision, and patient safety.
• Supportive culture with strong communication and commitment to excellence.
• Health and welfare benefits may be provided.
• Additional incentive plans, bonuses, or other compensation may be available depending on the position.