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

Coordinate multiple concurrent clinical trials as primary liaison between investigators, sponsors, and clinical staff. Manage subject scheduling and eligibility, maintain regulatory documentation, collect/process specimens, record adverse events, support audits, train staff, and ensure protocol and GCP compliance.

Supports clinical trial operations under the direction of Study Coordinators, including data entry, query resolution, document management, participant recruitment and enrollment, visit tracking, protocol-specific assessments, specimen collection, adverse event documentation, and volunteer education. Maintains compliance with GCP, SOPs, and study protocols while coordinating with investigators and research staff. Requires strong organization, communication, confidentiality, and attention to detail, with Spanish-English bilingual proficiency preferred.

Supports clinical trial operations under the direction of study coordinators by preparing documents, entering and resolving data, recruiting and educating research volunteers, tracking visits, maintaining study systems and supplies, and performing protocol-specific procedures such as vital signs, ECGs, medical histories, and specimen collection. Ensures compliance with GCP, SOPs, confidentiality requirements, and study protocols while documenting adverse events, communicating issues, and maintaining accurate source records.

Coordinate multiple concurrent clinical trials, serving as a liaison among investigators, sponsors, CROs, and clinical staff. Responsibilities include participant screening and scheduling, protocol compliance, study documentation, adverse-event reporting, specimen processing, supply tracking, staff training, sponsor communication, and audit preparation. The role also performs clinical procedures such as vital signs and ECGs, maintains regulatory records, and supports participant safety and privacy requirements. Bilingual English and Spanish communication is required.

Provides medical oversight for volunteers in clinical research studies, including screening, physical assessments, diagnostic interpretation, medication and treatment orders, adverse-event reporting, protocol execution, informed consent support, documentation, and volunteer management. Collaborates with Principal Investigators and multidisciplinary teams while ensuring compliance with clinical research regulations, Good Clinical Practice, HIPAA, and applicable protocols.

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 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.