Jobs at Innovo Research

Provide direct clinical care to research participants in clinical trials, including phlebotomy, vital sign monitoring, administering study interventions per protocol, adverse event assessment and reporting, scheduling and coordinating study visits, consenting assistance, specimen handling, regulatory documentation (IRB, SOPs), and training/auditing site staff while maintaining nursing licensure and compliance.

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.

Provide direct clinical care to research participants in trials, including phlebotomy, vitals, administering interventions per protocol, screening/recruiting/enrolling subjects, scheduling and coordinating study visits, collecting and documenting source data, reporting adverse events, preparing IRB submissions, handling investigational products and specimens, ensuring regulatory compliance, maintaining licensure and training, and supporting informed consent and staff training.

The Senior Clinical Research Coordinator will oversee clinical research operations, mentor staff, manage trials, and ensure compliance with regulations.

Coordinate and execute clinical study activities: enroll and consent participants, collect and maintain study data and source documentation, perform clinical procedures (phlebotomy, vitals, ECG, spirometry), handle lab logistics, monitor subject safety and adverse event reporting, support regulatory submissions and monitoring/audits, train site staff, and maintain study supplies and quality control per protocol, GCP/ICH, and FDA requirements.

The Clinical Research Assistant coordinates clinical trial protocols, ensures compliance, recruits participants, maintains records, and collaborates with a clinical team.

The Clinical Research Nurse conducts patient care for clinical trials, manages trials, monitors participant health, and ensures regulatory compliance.

The Clinical Research Assistant is responsible for coordinating clinical trial activities, maintaining documents, providing patient care, and ensuring regulatory compliance.