Jobs at Innovo Research

Coordinates daily operations for multiple clinical research trials, including screening, enrollment, scheduling, protocol procedures, documentation, data entry, query resolution, IRB submissions, specimen processing, and monitoring visits. Performs clinical functions, supports informed consent and participant safety, manages supplies and study documents, and mentors research staff. Ensures compliance with protocols, ICH GCP, regulations, SOPs, and sponsor requirements while collaborating with investigators, vendors, laboratories, and clinical teams.

Manages centralized regulatory operations across clinical research sites, including electronic regulatory binders, IRB submissions, informed consent forms, study-startup documents, training records, and audit readiness. Serves as a liaison for monitoring and site visits, supports inspections, assesses regulatory risks, and trains internal teams on protocol requirements. Requires knowledge of FDA regulations, ICH guidelines, and GCP standards, along with strong organization and communication skills.

Coordinates clinical research studies by recruiting and consenting participants, scheduling visits, collecting and maintaining study data, performing clinical procedures, managing specimens, monitoring safety, resolving data queries, and maintaining regulatory documentation. Supports investigators during study execution, audits, inspections, and monitoring visits while ensuring compliance with protocols, SOPs, GCP, FDA regulations, and quality standards. The role also trains site staff, manages supplies, coordinates coverage, and collaborates with provider offices.

Supports clinical trial operations from initiation through closeout, including participant recruitment, eligibility screening, informed consent, study visits, patient care, phlebotomy, specimen handling, documentation, regulatory compliance, and audit support. Maintains case report forms, source records, regulatory files, inventories, schedules, and electronic research systems. Collaborates with investigators, providers, sponsors, patients, and research staff while ensuring adherence to GCP, FDA, HIPAA, protocol, safety, confidentiality, and data-integrity requirements.

Identifies, screens, recruits, educates, and consents patients for clinical trials. Maintains recruitment and consent records, schedules appointments, supports participants, coordinates with investigators and healthcare professionals, and follows study protocols, regulatory requirements, and ethical standards. This is a fully on-site clinical office role with occasional evening or weekend work.

Provides direct patient care and clinical research support for multiple concurrent trials. Responsibilities include screening and enrolling participants, coordinating study visits, conducting health assessments, administering interventions within licensure, monitoring adverse events, collecting specimens, maintaining regulatory and source documentation, supporting IRB submissions, entering and resolving data queries, and training site staff. Requires an active nursing license, clinical research knowledge, strong organization, and adherence to protocol, safety, and regulatory requirements.

Coordinates daily operations for multiple clinical research trials, including participant screening, recruitment, enrollment, scheduling, protocol procedures, data entry, query resolution, specimen handling, IRB submissions, and essential document management. Performs clinical functions, supports informed consent and participant safety, mentors research staff, manages study supplies, and facilitates site qualification, initiation, monitoring, and close-out activities. The role requires compliance with GCP, regulatory requirements, sponsor policies, and IRB-approved protocols.

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.

Coordinates daily operations for multiple clinical trials, including participant screening, recruitment, enrollment, scheduling, clinical procedures, specimen processing, data entry, query resolution, and regulatory submissions. Maintains study documentation, supports informed consent and participant safety, manages supplies and vendors, and facilitates site qualification, initiation, monitoring, and close-out activities. Mentors staff and ensures compliance with protocols, ICH GCP, IRB requirements, sponsor policies, and applicable regulations.

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.

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 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.