Jobs at Elite Clinical Network

Serves as the first point of contact in a clinical trial clinic by answering calls, scheduling appointments, registering patients, explaining study information, and supporting clinical staff. Maintains accurate data entry, a welcoming reception area, and general office operations while assisting with patient recruitment and protocol-based scheduling.

Conducts Phase I-IV clinical trials as a Principal Investigator or Sub-Investigator while providing medical care to adult participants. Responsibilities include screening and enrolling patients, evaluating eligibility, overseeing safety and adverse events, maintaining regulatory documentation, collaborating with sponsors and research staff, participating in monitoring visits and audits, managing patient conditions, counseling participants, and supporting recruitment and retention.

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.

Conduct Phase I-IV clinical trials as a Principal or Sub-Investigator while providing medical care to adult patients. Responsibilities include screening and enrolling participants, evaluating eligibility, overseeing safety and adverse events, maintaining regulatory documentation, ensuring protocol compliance, collaborating with sponsors and research staff, participating in monitoring visits and audits, and supporting recruitment and retention.

Manages investigational product operations for clinical research studies, including sterile preparation, dispensing, blinding, inventory control, accountability, temperature monitoring, and regulatory documentation. Coordinates with investigators, site staff, and clinical research associates to maintain protocol, GCP, FDA, USP, and sponsor compliance. Supports monitoring visits, audit readiness, and safe handling of complex and hazardous medications.

Coordinates clinical trials and research studies by recruiting and enrolling participants, obtaining consent, collecting specimens, conducting basic procedures, maintaining study documentation, scheduling visits, supporting IRB submissions, and ensuring protocol, regulatory, and investigational product compliance. Communicates with sponsors, monitors, and IRBs while maintaining accurate records in clinical databases.

Leads day-to-day clinical research study operations from start-up through close-out, ensuring protocol compliance, data integrity, regulatory readiness, and accurate documentation. Recruits and supports participants, manages IRB submissions and EDC data, coordinates sponsors and monitors, and supports audits and inspections. Mentors and oversees clinical research coordinators, distributes workloads, reviews documentation, and escalates protocol or compliance issues. Requires occasional travel between sites and possible evening or weekend work.

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, screening, consent, scheduling, specimen collection, basic clinical procedures, data entry, regulatory documentation, and communication with sponsors, monitors, and IRBs. Ensures protocol compliance, accurate records, proper specimen and investigational product handling, and timely study visits.

Coordinates clinical trials and research studies, including participant recruitment, screening, consent, scheduling, specimen collection, basic clinical procedures, data entry, regulatory documentation, and IRB communications. Ensures protocol compliance, accurate records, investigational product accountability, and proper specimen handling while collaborating with sponsors, monitors, and multidisciplinary teams.

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, maintaining regulatory documentation, ensuring ICH-GCP and FDA compliance, collaborating with sponsors and research staff, participating in monitoring visits and audits, and supporting recruitment and retention.

Conducts Phase I–IV clinical trials as a Principal Investigator or Sub-Investigator while providing medical care to adult participants. Responsibilities include screening and enrollment assessments, eligibility evaluation, safety monitoring, adverse-event review, protocol compliance, clinical documentation, regulatory participation, patient counseling, recruitment, and retention. Requires an MD or DO, unrestricted medical license, Internal Medicine board certification or eligibility, and at least one year of clinical practice experience.

Coordinates clinical trials and research studies, including participant recruitment, screening, enrollment, informed consent, visit scheduling, specimen collection, basic clinical procedures, data entry, regulatory documentation, and investigational product accountability. The role communicates with sponsors, monitors, and IRBs while ensuring protocol compliance, accurate records, and ethical study conduct. Phlebotomy or Medical Assistant certification is preferred for specimen collection and clinical procedures.

Supports clinical research studies through participant screening, recruitment, scheduling, data entry, documentation, regulatory compliance, and study visit assistance. Maintains participant records and regulatory files, supports informed consent and noninvasive procedures, resolves data queries, and assists with audits and monitoring visits. Works under Clinical Research Coordinator and Principal Investigator supervision while following study protocols, GCP, HIPAA, IRB requirements, and institutional policies.

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.

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.

Oversee daily operations of a clinical research site including staff management, study execution from initiation to close-out, regulatory compliance (GCP/ICH), data integrity, financial oversight, recruitment/enrollment, vendor and sponsor communication, training, and continuous performance improvement to ensure timely, high-quality trial conduct.

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.