Independent Trials Lead - Clinical Research Coordinator II

Adams Clinical, Inc.; Dallas (TX); On-site; USD 34,000 - 41,000; 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, Inc. in Dallas is seeking a Clinical Research Coordinator II to join a rapidly growing site network focused on late-phase psychiatric and neurological trials, supporting inpatient and outpatient studies.

You will independently manage one or more complex trials under senior supervision, handling screening, enrollment, and regulatory readiness. A bachelor’s degree and at least 1 year of trial experience are required, with strong communication to sponsors.

Qualifications

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

Responsibilities

• Independently manage a portfolio of complex and/or high-volume trials with guidance from the Site Manager.
• Own study execution including screening operations, enrollment progress, and metrics.
• Conduct participant visits, clinical procedures, and eligibility assessments per protocol.
• Lead start-up activities for assigned studies and ensure regulatory readiness.
• Serve as primary liaison with sponsors, monitors, and CROs.
• Train and supervise CRC I/RA staff supporting the portfolio and maintain quality oversight.
• Lead data entry and query resolution to ensure data quality and inspection readiness.
• Maintain IP accountability, storage, dispensing, reconciliation, and disposal per SOPs.

Skills

Communication skills

Clinical trial coordination

Education

Bachelor's degree

1 year clinical research experience

Job description

Adams Clinical, Inc. in Dallas is seeking a Clinical Research Coordinator II to join a rapidly growing site network focused on late-phase psychiatric and neurological trials, supporting inpatient and outpatient studies.

You will independently manage one or more complex trials under senior supervision, handling screening, enrollment, and regulatory readiness. A bachelor’s degree and at least 1 year of trial experience are required, with strong communication to sponsors.