Jobs at Innovo Research

Entry-level role supporting clinical trials by coordinating recruitment, study visits, informed consent, phlebotomy and lab shipping; maintaining regulatory/source documents and EMR records; scheduling patients; collaborating with investigators and staff; and ensuring compliance with safety, confidentiality, and clinical research regulations.

Recruit and screen potential participants for clinical trials in the Champaign-Urbana area. Develop recruitment strategies, educate and consent candidates, maintain regulatory-compliant records, schedule appointments, coordinate with study teams, and provide ongoing participant support while adhering to ethical and institutional guidelines.

Provide direct nursing care to clinical trial participants, perform assessments, phlebotomy, administer interventions per protocol, monitor and report adverse events, manage recruitment/enrollment and study documentation, assist with informed consent, ensure regulatory compliance, and support training and coordination across study teams.

Provide direct clinical care to research participants in trials, including phlebotomy, assessments, administering interventions per protocol, monitoring/reporting adverse events, coordinating enrollment and study visits, maintaining source documentation and regulatory submissions, and ensuring participant safety and compliance with SOPs and licensure requirements.

Provide direct clinical care and safety monitoring for clinical trial participants; screen, recruit, enroll, schedule and assess subjects; collect and document clinical data and specimens; manage investigational product handling, adverse event reporting, IRB submissions, and training; maintain regulatory compliance and active nursing licensure.

Coordinate and manage clinical study activities: recruit and consent subjects, collect and maintain research data and regulatory documents, perform clinical procedures (phlebotomy, ECG, spirometry, vitals), handle specimen logistics, monitor safety and report adverse events, support audits/monitoring, and train/coordinate site staff to ensure protocol and regulatory compliance.

Coordinate and manage clinical study activities including participant recruitment and consent, data collection and QC, regulatory documentation, specimen handling, clinical procedures (phlebotomy, ECG, spirometry), adverse event reporting, scheduling, and support for monitoring, audits, and site staff training.

Entry-level role supporting clinical trials by coordinating recruitment, consent, study visits, regulatory documentation, specimen handling, data recording, patient care (including phlebotomy), scheduling, and collaboration with investigators and staff to ensure protocol compliance.

The Clinical Research Coordinator manages clinical research data and assists with clinical trials by recruiting participants, maintaining documentation, and ensuring protocol adherence.

The Part-Time Sales Representative/Manager will identify and close data opportunities with pharmaceutical and biotech companies, manage key accounts, and achieve revenue targets.