Jobs at Elite Clinical Network

Coordinates clinical research data and source documentation across clinical operations, contracts, study sites, and CTMS teams. Interprets clinical trial agreements, performs system data entry, reviews CTMS templates, develops standardized source documents, supports system integration, addresses audit findings, and provides site troubleshooting. Ensures documentation accuracy, regulatory compliance, data integrity, and alignment with protocol requirements across multiple studies.

Coordinate and support clinical trials by recruiting and consenting participants, collecting and processing specimens, performing basic clinical procedures, maintaining regulatory documentation and electronic case report forms, communicating with sponsors/IRBs, and ensuring protocol compliance and visit scheduling.

Coordinate and support clinical trials including recruitment, informed consent, specimen collection and handling, regulatory documentation, data entry in EDC/REDCap, scheduling visits, and communication with sponsors, monitors, and IRBs.

Manages day-to-day clinical study operations from start-up to close-out, ensuring protocol, IRB, FDA, and GCP compliance; oversees recruitment, consenting, data entry in EDC, regulatory documentation, audit readiness, and mentors/coordinates the CRC team.

Manage day-to-day clinical study operations, ensure protocol and regulatory compliance, enroll and follow participants, maintain accurate EDC and regulatory documentation, support audits, and lead/mentor coordinator team.

Oversee daily operations of a clinical research site, ensuring compliance with GCP/ICH, managing staff and budgets, meeting enrollment targets, maintaining data integrity, liaising with sponsors/CROs, and driving site performance and audit readiness.

Provide clinical care and medical oversight as Principal Investigator or Sub-Investigator on Phase I-IV dermatology trials. Screen and enroll patients, perform exams, assess eligibility and safety, document per ICH-GCP/FDA requirements, collaborate with coordinators and sponsors, support recruitment and retention, and participate in site visits, monitoring, and audits.

Provide travel-based operational support to East Coast clinical trial sites: manage startup, patient recruitment, screening, consent, study visits, EDC entry, IRB submissions, regulatory binders, monitoring/audit readiness, and train/onboard site staff while coordinating travel logistics and ensuring GCP compliance.

Provide on-site operational support for clinical trial startup and early enrollment at California sites. Travel to manage recruitment, consent, visits, data entry, regulatory documentation, and site readiness. Train and support site staff, maintain regulatory binders, ensure GCP compliance, assist monitoring and audits, and coordinate logistics to drive enrollment and study execution.

Traveling clinical research coordinator responsible for site start-up, participant recruitment, protocol adherence, data capture, regulatory/IRB submissions, monitoring/audit readiness, and training site staff. Provides operational support during high-enrollment periods and manages travel logistics while ensuring GCP and FDA compliance.

First-line IT support handling high-volume helpdesk requests via Freshservice. Troubleshoot Windows and macOS hardware/software, support Microsoft 365, assist with device provisioning using Intune/Autopilot, manage accounts in Entra ID, support remote users, document resolutions, perform basic network troubleshooting, contribute to the IT knowledge base, and assist on IT projects and onboarding/offboarding.

Provide operational support to Arizona research sites during startup and early enrollment by traveling to manage recruitment, screening, consent, study visits, regulatory documentation, EDC entry, and site training. Ensure GCP/FDA compliance, maintain regulatory binders, support monitoring/audits, coordinate logistics and inventory, and onboard/train site staff.

Manage and coordinate clinical research studies from start-up to close-out, ensuring protocol compliance, data integrity, IRB submissions, EDC data entry, participant recruitment/consent, regulatory documentation, audit readiness, and serve as site-level mentor and escalation resource for coordinator staff.

Coordinate and support clinical trials including participant recruitment, consenting, scheduling, specimen collection/processing/shipping, basic clinical procedures, data entry in EDC systems, regulatory document maintenance, and communication with sponsors/monitors/IRBs to ensure protocol compliance.

Coordinate and support clinical trials including participant recruitment, consent, specimen collection and processing, documentation, regulatory compliance, scheduling, and communication with sponsors/IRBs. May perform basic clinical procedures if certified.

Provide clinical care and medical oversight for adult participants in Phase I-IV trials as Principal Investigator or Sub-Investigator. Conduct exams, assess eligibility, manage safety and adverse event reporting, ensure protocol compliance and regulatory documentation (ICH-GCP, FDA), collaborate with study teams and sponsors, support recruitment and retention, and participate in site visits, monitoring, and audits.

Serve as Principal Investigator or Sub-Investigator on Phase I-IV trials, perform clinical assessments, evaluate eligibility, provide medical oversight and safety monitoring, maintain ICH-GCP/FDA-compliant documentation, support recruitment and retention, and collaborate with coordinators, sponsors, and monitors.

Support clinical study execution by assisting with study materials, participant screening and scheduling, data entry into eCRFs/EDC, regulatory document maintenance, informed consent support, and participation in audits and team activities to ensure GCP and HIPAA compliance.

Coordinate day-to-day clinical trial activities including participant recruitment, informed consent, specimen collection/handling, basic clinical procedures, regulatory document maintenance, data entry in EDC/REDCap, and communication with sponsors, monitors, and IRBs to ensure protocol compliance.

The Site Manager oversees clinical trial execution, ensures compliance, manages budgets, and leads site staff while maintaining data integrity and participant recruitment.