CRC II: Lead High-Volume Trials (Dallas)

Adams Clinical; Dallas (TX); On-site; USD 47,000 - 59,000; Full time

Benefits offered by this job

401(k) matching

Medical, Dental, & Vision insurance

Employee assistance program

Flexible spending account

Health insurance

Health savings account

Life insurance

Paid time off

Parental leave

Professional development assistance

Job summary

Adams Clinical invites applications for a Clinical Research Coordinator II at our Dallas location. You will manage complex or high-volume trials, oversee study conduct, and ensure operational excellence under supervision, contributing to data integrity and regulatory readiness.

The role emphasizes protocol mastery, collaboration with sponsors and CROs, and leadership of CRC I/RA teammates. A Bachelor’s degree and 1 year of industry-sponsored clinical trials experience are required.

Qualifications

• Bachelor’s degree required.
• At least 1 year of prior clinical research experience.
• Experience with industry-sponsored clinical trials required.
• Demonstrated ability to manage complex studies independently.
• Strong communication skills and comfort interacting directly with sponsors.

Responsibilities

• Independently manage a portfolio of complex and/or high-volume trials with guidance from a CRC III or the Site Manager, leading all operational and visit-related activities.
• Fully own study execution, including screening operations, enrollment progress, screening vs. target metrics, and SCF rates.
• Conduct all participant visits, clinical procedures, and eligibility assessments per protocol.
• Lead study start-up activities for assigned studies, including SIV preparation, regulatory readiness, supply planning, and supporting site completion of required staff training.
• Serve as the primary liaison with study sponsors, monitors, and CROs.
• Review source and eligibility criteria to ensure accurate screening and enrollment decisions.
• Train and supervise CRC I's or RAs supporting the portfolio; maintain quality and performance oversight.
• Lead data entry and query resolution efforts, ensuring high data quality and inspection readiness.
• Maintain investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and proper disposal, ensuring compliance with protocol, regulatory requirements, and site SOPs.
• Identify operational risks and propose corrective actions to maintain study timelines and quality.
• Compile study metrics across assigned trials, including enrollment progress, screening performance, visit completion, and data quality.
• Prepare internal performance summaries for the site team and escape issues or trends to senior staff.
• Present study metrics and operational updates to sponsors, monitors, or CRO leadership for assigned trials.
• Serve as a point of contact for resolving data queries and ensuring inspection readiness.

Skills

Clinical research experience

Independent study management

Strong communication skills

Education

Bachelor’s degree

Job description

Adams Clinical invites applications for a Clinical Research Coordinator II at our Dallas location. You will manage complex or high-volume trials, oversee study conduct, and ensure operational excellence under supervision, contributing to data integrity and regulatory readiness.

The role emphasizes protocol mastery, collaboration with sponsors and CROs, and leadership of CRC I/RA teammates. A Bachelor’s degree and 1 year of industry-sponsored clinical trials experience are required.