Dynamic Clinical Trials Coordinator II (Multi-Study Focus)

Johnson County Clin Trials (JCCT); Lenexa (KS); On-site; USD 55,000 - 90,000; Full time

Job summary

Johnson County Clin Trials (JCCT) seeks a Clinical Research Coordinator II to oversee overlapping clinical studies and serve as the primary contact for sponsors. The role emphasizes protocol compliance, regulatory documentation, and cross-functional collaboration with investigators, staff, and QA.

You will manage enrollment, data collection, adverse events, and study visits while maintaining ALCOA+ compliant source documentation.

Qualifications

• BS/BA in Life Science or related discipline; CFR, GCP, HIPAA basics.
• Minimum 3 years coordinating clinical trials with overlapping timelines.
• CCRC certification a plus; nursing/medical assistant background helpful.
• Demonstrated ability to build relationships with sponsors and site staff.
• Ability to explain GCP guidelines and train others on protocols.

Responsibilities

• Coordinate multiple concurrent trials and be main sponsor contact.
• Maintain study logs, case report forms, and regulatory forms.
• Educate volunteers on procedures and ICF process.
• Ensure protocol amendments and training documentation are complete.
• Collaborate with QA and regulatory teams for audits.

Skills

Communication skills

Interpersonal skills

Analytical skills

Problem-solving

Time management

Organizational skills

Detail oriented

Teamwork

Self-motivated

Critical thinking

Education

BS/BA in Life Science or related discipline

3 years clinical trials coordination experience

CCRC certification a plus

Nursing/medical assistant experience a plus

Regulatory knowledge CFR/GCP/HIPAA

Tools

Medidata Rave

Inform

TrialKit

MS Office (Outlook/Word/Excel/PowerPoint/SharePoint)

Job description

Johnson County Clin Trials (JCCT) seeks a Clinical Research Coordinator II to oversee overlapping clinical studies and serve as the primary contact for sponsors. The role emphasizes protocol compliance, regulatory documentation, and cross-functional collaboration with investigators, staff, and QA.

You will manage enrollment, data collection, adverse events, and study visits while maintaining ALCOA+ compliant source documentation.