Jobs at Johnson County Clin-Trials, L.L.C.

Serves as the first point of contact for patients, study participants, sponsors, and visitors. Greets guests, manages phone calls, supports check-in and check-out, schedules appointments, maintains accurate records, protects patient privacy, and keeps reception and patient areas organized. The role also coordinates with administrative staff to improve visitor support and front-office processes.

Coordinates multiple concurrent clinical trials, serving as a liaison among investigators, sponsors, CROs, clinical staff, and volunteers. Responsibilities include participant screening and scheduling, protocol and regulatory documentation, study procedures, specimen handling, adverse-event reporting, enrollment tracking, team training, sponsor communication, audit preparation, and maintaining compliance with GCP, HIPAA, IRB, and safety requirements.

Coordinates multiple concurrent clinical trials, serving as a liaison among investigators, sponsors, CROs, clinical staff, and volunteers. Responsibilities include participant screening and scheduling, protocol and regulatory compliance, study documentation, adverse-event reporting, specimen handling, data entry, staff training, sponsor communication, site visits, and audit preparation. The role also performs clinical procedures such as vital signs and ECGs while maintaining participant safety, privacy, and high-quality research standards.

Coordinate multiple concurrent clinical trials as primary liaison for sponsors and investigators. Manage recruitment, scheduling, regulatory documentation, specimen handling, AE reporting, QA audits, and team training while ensuring protocol and GCP compliance. Bilingual (English/Spanish) communication with patients and staff required.

Coordinate multiple concurrent clinical trials in nephrology, serving as primary liaison with investigators, sponsors, and clinical staff. Manage subject recruitment and enrollment, eligibility assessments, regulatory documentation, data entry in EDC systems, specimen collection/processing, adverse event reporting, site audits, mentoring staff, and ensuring GCP/CFR/HIPAA compliance.

Lead and oversee clinical site operations, ensuring regulatory compliance (GCP/FDA/ICH), study start-up and execution, vendor and sponsor liaison, staff training and mentoring, KPI reporting, and readiness for audits and inspections.

The Sub-Investigator conducts medical evaluations and manages volunteer health in clinical research studies, ensuring adherence to protocols and participant welfare.