Jobs at Innovo Research

Identify, screen, recruit, and consent patients for clinical trials; develop recruitment strategies; maintain records; coordinate with clinical teams; ensure regulatory compliance and participant support.

Provide direct clinical care and safety monitoring for clinical trial participants, perform procedures (phlebotomy, vitals), manage enrollment and study visits, collect and document data, report adverse events, assist with informed consent and investigational product handling, and maintain regulatory compliance and training.

Provide direct patient care and clinical trial support: screening, enrollment, assessments, administering interventions per protocol, monitoring/reporting adverse events, specimen handling, regulatory documentation, and training site staff.

Provide patient-facing support for clinical studies: obtain consent, screen and recruit participants, perform study visits and delegated procedures (phlebotomy), document CRFs and regulatory records, manage specimens and supplies, support monitoring/audits, and maintain compliance with GCP, FDA, HIPAA and site SOPs.

Support clinical trial activities including participant recruitment and screening, informed consent, study visits, specimen handling, regulatory documentation, CTMS/EMR data entry, coordination with investigators and sponsors, adherence to GCP/FDA/HIPAA, and general site administrative tasks to ensure study compliance and patient safety.

Coordinate daily operations of multiple clinical trials, mentor staff, perform clinical procedures when needed, manage recruitment/scheduling, maintain source documentation and regulatory submissions (IRB, GCP/ICH compliance), support specimen handling and study logistics, and liaise with sponsors, vendors, and partner clinics while ensuring participant safety and protocol adherence.

Coordinate and oversee daily operations of clinical trials, including participant screening, enrollment, consenting, specimen collection, data entry, regulatory/IRB submissions, staff mentoring, and site management to ensure GCP-compliant execution of multiple concurrent studies.

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.

Coordinate and manage clinical trial activities including participant recruitment, consent, data collection and regulatory documentation; perform clinical procedures (phlebotomy, vitals, ECG, spirometry), ensure protocol and GCP compliance, assist with monitoring/audits, maintain source documents, and support investigator site operations.

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

Coordinate and execute clinical research studies: recruit and consent participants, collect and maintain study data and source documentation, perform clinical procedures (phlebotomy, ECG, spirometry, vitals), manage regulatory submissions and study supplies, support monitoring/audits, ensure GCP/ICH and FDA compliance, report adverse events, and train site staff.