Jobs at Elite Clinical Network

Conduct Phase I–IV clinical trials as a Principal or Sub-Investigator while providing dermatologic care to adult participants. Responsibilities include screening and enrolling patients, assessing eligibility, overseeing safety and adverse events, documenting clinical and regulatory data, ensuring ICH-GCP and FDA compliance, collaborating with sponsors and research staff, participating in monitoring visits and audits, counseling patients, and supporting recruitment and retention.

Coordinates clinical trials and research studies, including participant recruitment, screening, informed consent, visit scheduling, specimen collection, basic clinical procedures, data entry, regulatory documentation, and communication with sponsors, monitors, and IRBs. Ensures protocol adherence, ethical conduct, accurate records, specimen accountability, and compliance with clinical research requirements.

Coordinates clinical trials and research studies, including participant recruitment, informed consent, visit scheduling, specimen collection and processing, clinical procedures, data entry, regulatory documentation, investigational product accountability, and communication with sponsors, monitors, and IRBs. Ensures protocols, ethical standards, GCP requirements, and visit windows are followed while maintaining accurate study records.

The Dermatologist will conduct clinical trials, assess patient eligibility, provide medical oversight, and collaborate with research teams while delivering patient care.

The Gastroenterologist will conduct clinical trials as Principal Investigator or Sub-Investigator, provide patient care, and ensure protocol compliance.

The Physician - Rheumatologist will serve as a Principal or Sub-Investigator in clinical trials, provide patient care, ensure protocol compliance, and manage chronic and acute conditions.

The Clinical Research Coordinator will manage clinical trials by recruiting participants, collecting data, ensuring compliance, and maintaining documentation.

The Physician - Endocrinologist will conduct clinical trials, oversee patient care, collaborate with research teams, and manage trial documentation while ensuring patient safety and protocol 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.

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

The Site Manager oversees clinical trial operations, manages site staff, ensures compliance, and coordinates resources for successful study execution.

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.