Clinical Research Coordinator II (CRC II) -- research nurse preferred
Location: Plano, TX (Travel between DFW sites required)
Job Type: Full-Time
About ACRC Trials
ACRC Trials is a growing multi-site clinical research organization committed to advancing medicine through high-quality clinical trials. We pride ourselves on operational excellence, patient safety, and a collaborative team culture. As we continue to expand, we're looking for experienced Clinical Research Coordinators who thrive in a fast-paced environment and are passionate about research.
Position Summary
The Clinical Research Coordinator II (CRC II) independently manages assigned clinical trials while ensuring protocol compliance, regulatory excellence, and outstanding participant care. This role requires an experienced coordinator who can confidently manage studies from startup through closeout while serving as a primary point of contact for sponsors, monitors, vendors, and study participants.
The ideal candidate is organized, proactive, accountable, and committed to delivering high-quality clinical research.
What You'll Do
- Independently manage multiple clinical research studies from enrollment through study completion
- Coordinate participant recruitment, screening, enrollment, scheduling, and retention
- Conduct study visits and protocol-required procedures within delegated scope
- Perform accurate source documentation, EDC data entry, and query resolution
- Maintain inspection-ready regulatory and study documentation
- Coordinate laboratory processing, specimen shipping, and investigational product accountability
- Serve as the primary contact for sponsors, CRAs, central vendors, and study participants
- Prepare for sponsor monitoring visits, audits, and inspections
- Identify and report protocol deviations, adverse events, and serious adverse events
- Support participant safety and ensure compliance with ICH-GCP, FDA regulations, sponsor requirements, and site SOPs
- Mentor and provide day-to-day support for junior coordinators when appropriate
- Collaborate across departments to ensure efficient study execution
- Travel between ACRC Trials locations as needed
QualificationsRequired
- Minimum 2 years of Clinical Research Coordinator experience
- Experience coordinating industry-sponsored clinical trials
- Strong knowledge of ICH-GCP guidelines
- Experience with EDC systems
- Excellent organizational and time management skills
- Strong communication and interpersonal abilities
- Ability to independently prioritize multiple studies
- Proficient with Microsoft Office
- RN certification is a +
Preferred
- Experience with CRIO
- Experience with Clinical Conductor (CC)
- Experience across multiple therapeutic areas
- Phlebotomy and ECG experience
- BLS certification
What We're Looking For
We are looking for someone who is:
- Highly organized and detail-oriented
- Able to work independently with minimal supervision
- Patient-focused and compassionate
- Comfortable in a fast-paced environment
- Solutions-oriented with excellent critical thinking skills
- Responsive and accountable
- A strong team player who enjoys collaboration
Why Join ACRC Trials?
- Competitive salary
- Medical, dental, and vision benefits
- Paid Time Off
- Paid holidays
- 401(k)
- Professional development opportunities
- Opportunity to work on cutting-edge clinical research
- Collaborative leadership team
- Growing organization with opportunities for advancement
Experience
- Clinical Research Coordinator: 2 years (Required)
License/Certification
- BLS Certification (Preferred)
Work Location
In Person
Pay: $62,730.46 - $75,546.36 per year
Work Location: In person
