Clinical Research Coordinator II

Dallasfull timeOn Site

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mid

$48k–$59k

H1B: no

Adamsclinical Clinical Research Coordinator II at Adams Clinical independently manages complex or high-enrolling clinical trials, overseeing study execution and operational outcomes. The role includes supervising junior staff and serving as the primary liaison with sponsors and monitors.

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 RA's 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 escalate issues or trends to senior staff.

Qualification

Bachelor’s degree requiredPay

Required

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.
Pay: $23.00 - $28.37 per hour