Jobs at Elite Clinical Network

Support execution of clinical research studies by assisting with study coordination, participant screening and consent, data entry into eCRFs, regulatory document maintenance, and ensuring GCP/HIPAA compliance while collaborating with clinical teams and participating in audits and quality reviews.

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.

Coordinate day-to-day clinical research activities including participant recruitment, informed consent, specimen collection/processing, basic clinical procedures, data entry in EDC systems, regulatory document maintenance, IRB communications, and sponsor/monitor liaison to ensure protocol compliance and timely study visits.

Coordinate and support clinical trials including participant recruitment, informed consent, specimen collection and processing, data entry in EDC, regulatory documentation, scheduling visits, and communication with sponsors, monitors, and IRBs. May perform basic clinical procedures and ensure protocol compliance and investigational product accountability.

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

The Clinical Research Coordinator will manage clinical trials by coordinating participant recruitment, data collection, regulatory compliance, and specimen handling, ensuring adherence to protocols.

The Physician - Internist will serve as Principal or Sub-Investigator on clinical trials, providing medical care, evaluating patients, and ensuring protocol compliance.

The Physician - Dermatologist will serve as Principal or Sub-Investigator on clinical trials, provide medical care to patients, and ensure protocol compliance.

Coordinate and support clinical trials including recruitment, informed consent, specimen collection and processing, data entry, regulatory compliance, scheduling, and communication with sponsors/IRBs. May perform basic clinical procedures and maintain regulatory documentation.

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

The Pulmonologist will oversee clinical trials, performing exams, assessing patient eligibility, ensuring protocol compliance, and providing patient care in a research environment.

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 Clinical Research Coordinator will manage clinical trials, including participant recruitment, data collection, regulatory compliance, and specimen handling, ensuring all protocols are followed.

Join the Elite Clinical Network as a Gastroenterologist, serving as PI or Sub-Investigator on clinical trials and providing medical care to patients.

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

The Physician - Endocrinologist will oversee clinical trials, evaluate patient eligibility, ensure compliance, manage patient care, and collaborate with research teams.

The Site Manager oversees clinical trial operations, manages site staff, ensures compliance with regulations, and monitors performance metrics, while ensuring financial health and managing study execution.

The Physician - Endocrinologist will conduct clinical trials as a Principal Investigator, manage patient care, and ensure compliance with medical protocols while collaborating with research teams.

The Gastroenterologist will lead clinical trials as Principal Investigator, perform patient assessments and evaluations, and ensure compliance with trial protocols while providing medical care.

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