Clinical Research Coordinator II

Adams Clinical•Dallas, TX

12h•$25 - $30•Onsite

About The Position

Adams Clinical is a clinical trial site network conducting late-phase, industry-sponsored clinical 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, with guidance from a CRC III or Site Manager. The coordinator is accountable for screening performance, study conduct, and operational outcomes and may supervise CRC Is or research assistants supporting assigned studies. The role requires strong protocol knowledge, clinical skills, and study-management capabilities.

Requirements

Bachelor’s degree required.
At least one year of experience as a clinical research coordinator on industry-sponsored trials.
Demonstrated ability to manage complex studies independently.
Comfort with seeing 12–20 participant visits per day.
Strong communication skills and comfort interacting directly with sponsors.

Nice To Haves

Experience with neurological and/or psychiatric patient populations.

Responsibilities

Independently manage a portfolio of complex and/or high-volume trials, leading operational and participant-visit 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 in accordance with study protocols.
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 documentation and eligibility criteria to support accurate screening and enrollment decisions.
Train and supervise CRC Is or research assistants and maintain quality and performance oversight.
Lead data entry and query resolution to ensure data quality and inspection readiness.
Maintain investigational product accountability, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and disposal in accordance with protocols, regulations, and site SOPs.
Identify operational risks and propose corrective actions to maintain study timelines and quality.
Compile study metrics, 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.