Clinical Research Coordinator II
Adams Clinical • Dallas, TX2d
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Clinical Research Coordinator II
Adams Clinical•Dallas, TX
About The Position
Adams Clinical is a clinical trial site network focused on late-phase, industry-sponsored research for psychiatric and neurological conditions, including inpatient and outpatient studies. The Clinical Research Coordinator II independently manages one or more complex or high-enrolling trials, taking ownership of screening performance, study conduct, and operational outcomes. The coordinator works under guidance from a CRC III or Site Manager and may supervise CRC Is or research assistants supporting their portfolio. The role involves coordinating study operations and participant visits, ensuring protocol compliance, data quality, and inspection readiness, and serving as a primary contact for sponsors, monitors, and CROs. The position is based at the Dallas location. The role is suited to an experienced coordinator who has managed multiple trials, supported or trained others, and collaborated with research staff.
Requirements
- Bachelor’s degree required.
- At least 1 year of prior experience as a clinical research coordinator on industry-sponsored trials.
- Demonstrated ability to manage complex studies independently.
- Comfortable seeing 12–20 participant visits per day.
- Strong communication skills and comfort interacting directly with sponsors.
Nice To Haves
- Experience with neuro and/or psychiatric patient populations.
Responsibilities
- Independently manage a portfolio of complex and/or high-volume trials, leading operational and visit-related activities with guidance from a CRC III or Site Manager.
- Own study execution, including screening operations, enrollment progress, screening-versus-target metrics, and SCF rates.
- Conduct participant visits, clinical procedures, and eligibility assessments according to protocol.
- Lead study start-up activities, including SIV preparation, regulatory readiness, supply planning, and support for required staff training.
- Serve as the primary liaison with study sponsors, monitors, and CROs.
- Review source information and eligibility criteria to support accurate screening and enrollment decisions.
- Train and supervise CRC Is or research assistants supporting the portfolio, and oversee quality and performance.
- Lead data entry and query resolution to maintain high data quality and inspection readiness.
- Maintain investigational product accountability, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and disposal in compliance with protocols, regulations, 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 and escalate issues or trends to senior staff.
- Present study metrics and operational updates to sponsors, monitors, or CRO leadership.
- Resolve data queries and support inspection readiness.
Benefits
- 401(k) matching
- Medical, dental, and vision insurance
- Employee assistance program
- Flexible spending account
- Health savings account
- Life insurance
- Paid time off
- Parental leave
- Professional development assistance
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
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