Clinical Trial Team
Physician-supervised roles that may work directly on future trials — once a protocol, IRB approval, training, and delegation authorize the activity.
Who belongs here: Principal investigators, study physicians, research nurses, coordinators, safety monitors, recruitment and screening staff, research pharmacists, telehealth coordinators.
17 roles
Principal Investigator
Clinical & participant safety · Leads a future study at a site: protocol conduct, participant safety, and data integrity under GCP. Full CV, active license, prior PI and IRB history, and conflict disclosure.
Sub-Investigator
Clinical & participant safety · Supports the PI on delegated study tasks under supervision. License/credential, GCP/HSP training, and clinical-research experience.
Study Physician / Supervising Physician
Clinical & participant safety · Provides clinical oversight: eligibility, adverse-event review, and participant safety. Active license, specialty, and protocol-specific availability.
Medical Monitor
Clinical & participant safety · Independent medical oversight and safety escalation across a study. Medical license, safety-monitoring experience, and independence attestation.
Clinical Research Nurse
Clinical & participant safety · Delivers study visits: vitals, specimen collection, dosing support, and source documentation. RN license, GCP/HSP, and research-nursing experience.
Nurse Practitioner / Physician Assistant
Clinical & participant safety · Advanced-practice support within scope and supervision arrangements. License, state scope, GCP/HSP, and clinical-research experience.
Clinical Research Coordinator
Clinical & participant safety · Coordinates recruitment, screening, consent logistics, visit scheduling, source documentation, and EDC entry after protocol-specific training and authorization.
Senior / Lead Clinical Research Coordinator
Clinical & participant safety · CRC experience plus team leadership, site startup, monitoring response, and delegation-log management.
Informed Consent Specialist
Clinical & participant safety · Supports legally effective, plain-language informed consent and its documentation. HSP/GCP, consent-process experience, and language skills.
Participant Navigator
Clinical & participant safety · Helps participants understand logistics and access support, within strict boundaries. Participant-support experience and language skills.
Recruitment & Screening Coordinator
Clinical & participant safety · Runs compliant recruitment and pre-screening with privacy training and approved scripts.
Research Pharmacist / Investigational Product Lead
Clinical & participant safety · Investigational-product accountability: storage, blinding, randomization support, and dispensing records. Pharmacist license where applicable.
Pharmacovigilance / Safety Specialist
Clinical & participant safety · Adverse-event reporting, MedDRA coding, and safety narratives under GCP/safety training.
Telehealth Study Coordinator
Clinical & participant safety · Remote visit and remote-consent workflows with privacy training and clear escalation paths.
Chief Medical Officer / Medical Director
Executive & scientific leadership · Clinical and safety leadership across the program. Medical CV, active license, board certification, GCP/HSP, and conflict disclosure.
Director of Clinical Operations
Executive & scientific leadership · Owns trial operations: SOPs, EDC/CTMS, site management, and inspection readiness.
Clinical Research Intern
Fellowship & early-career bench · Mentored, educational exposure to clinical research operations. Not a substitute for paid staff.