Jobs at Elite Clinical Network

Join as a Physician - Dermatologist, serving as Principal Investigator on clinical trials while providing quality care to patients, ensuring protocol compliance and patient safety.

The Physician - Pulmonologist conducts clinical trials, performs assessments, evaluates patient eligibility, provides medical oversight, and collaborates with research teams.

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.

Manage investigational product operations for clinical trials including sterile compounding, preparation and dispensing of IV, SC, and oral IPs. Ensure protocol/blinding adherence, maintain accountability logs, manage inventory and temperature monitoring, support monitoring/audit visits, and comply with FDA, GCP, and USP standards.

Entry-level, 12-18 month development role supporting daily clinical site operations and regulatory compliance. Assist with scheduling, visit coordination, data entry, regulatory documentation, recruitment tracking, and sponsor/CRO communications while shadowing site leadership to build supervisory, operational, and budgeting skills toward a Site Manager role.

Leads end-to-end clinical study start-up activities from pre-award through Greenlight activation. Coordinates regulatory approvals, essential documents, contracts, budgets, vendors, recruitment readiness, and cross-functional handoffs. Tracks milestones, manages workflow systems, escalates delays, supports performance reporting, and drives process improvements. Serves as a subject-matter expert and mentor while partnering with leadership to improve study activation timelines and recruitment performance.

Plans, launches, and optimizes paid digital advertising campaigns for clinical trial patient recruitment. Manages Google, Meta, and other advertising platforms; monitors budgets, lead quality, conversion metrics, and enrollment performance; and produces reporting for leadership. Creates compliant patient-facing scripts, ad copy, email and SMS templates, landing-page content, and visual materials using Canva. Maintains asset libraries and approval tracking while coordinating with recruitment teams, site managers, sponsors, and IRBs.

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.