Clinical Research Coordinator II — Lead High-Volume Trials

Adams Clinical, Inc.; Dallas (TX); On-site; USD 34,000 - 41,000; Full time

Benefits offered by this job

401(k) matching

Employee assistance program

Flexible spending account

Health insurance

Health savings account

Life insurance

Paid time off

Parental leave

Job summary

Adams Clinical, Inc. in Dallas is seeking an experienced Clinical Research Coordinator II to manage one or more trials, oversee day-to-day study operations, and collaborate with research staff under guidance from senior team members.

The CRC II will independently manage complex or high-enrolling trials, supervise CRC I's or RAs, ensure protocol mastery, conduct visits, screenings, and data entry, while maintaining regulatory readiness and data quality.

Qualifications

• At least 1 year of prior clinical research experience on industry-sponsored trials.
• Ability to manage complex studies independently.
• Strong communication skills, especially with sponsors.

Responsibilities

• Independently manage a portfolio of complex/high-volume trials with guidance from senior staff.
• Oversee screening, enrollment progress, and visit-related activities.
• Lead study start-up activities, regulatory readiness, and staff training.
• Serve as primary liaison with sponsors, monitors, and CROs.
• Train and supervise CRC I or RA staff supporting the portfolio.
• Ensure data entry accuracy and investigation readiness.
• Maintain IP accountability and regulatory compliance.
• Prepare internal performance summaries and present updates to stakeholders.

Skills

Clinical research experience

Independent trial management

Sponsor communication

Job description

Adams Clinical, Inc. in Dallas is seeking an experienced Clinical Research Coordinator II to manage one or more trials, oversee day-to-day study operations, and collaborate with research staff under guidance from senior team members.

The CRC II will independently manage complex or high-enrolling trials, supervise CRC I's or RAs, ensure protocol mastery, conduct visits, screenings, and data entry, while maintaining regulatory readiness and data quality.