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Clinical Research Coordinator (Unblinded Team Preferred)

ACRC TRIALS - 2.2

Plano, TX Job Details Full-time From $60,000 a year 4 hours ago Benefits Paid holidays Health insurance Dental insurance 401(k) Paid time off Vision insurance Opportunities for advancement Qualifications Teamwork Regulatory compliance Research project coordination ICH guidelines Medical research Attention to detail Patient care Organizational skills Productivity software Clinical quality assurance standards Clinical trial support in drug product development Time management Full Job Description Clinical Research Coordinator II -

Unblinded Team 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, participant safety, and a collaborative team culture. As we continue to expand, we are looking for experienced Clinical Research Coordinators who thrive in a fast-paced environment and are passionate about clinical 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. We prefer candidates with experience working on an unblinded study team , including investigational product accountability, preparation, administration, documentation, and maintenance of study blinding. Candidates who are appropriately licensed or qualified and comfortable administering injections to participants in vaccine studies are strongly preferred. 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 Support unblinded study activities while maintaining protocol-required blinding Coordinate investigational product receipt, storage, temperature monitoring, preparation, administration, accountability, and reconciliation Administer vaccines or other injectable study products within the individual's qualifications, licensure, delegated scope, protocol requirements, and site procedures Coordinate participant recruitment, screening, enrollment, scheduling, and retention Conduct study visits and protocol-required procedures within delegated scope Complete 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 a 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 compliance with

ICH-GCP, FDA

regulations, sponsor requirements, and site SOPs Mentor and provide day-to-day support to junior coordinators when appropriate Collaborate across departments to support efficient study execution Travel between ACRC Trials locations as needed Required Qualifications Minimum 2 years of Clinical Research Coordinator experience Experience coordinating industry-sponsored clinical trials Strong knowledge of ICH-GCP guidelines Experience using EDC systems Excellent organizational and time-management skills Strong communication and interpersonal abilities Ability to independently prioritize and manage multiple studies Proficiency with Microsoft Office Preferred Qualifications Previous experience working on an unblinded clinical research team Vaccine-study or investigational product administration experience Appropriate clinical qualification or licensure to administer injections Willingness and comfort administering vaccines to study participants RN, LVN/LPN, or other applicable clinical license Experience with CRIO Experience with Clinical Conductor 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 administering injections, when qualified and delegated Comfortable working in a fast-paced environment Solutions-oriented with strong critical-thinking skills Responsive and accountable A strong team player who enjoys collaboration Able to maintain study blinding and confidential unblinded information 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) Unblinded or vaccine-study experience: Preferred License/Certification Clinical license or qualification permitting injection administration:

Preferred BLS Certification:

Preferred Work Location In person, with travel between ACRC Trials locations as needed.

Pay:

From $60,000.00 per year

Work Location:

In person