Jobs at ObjectiveHealth

Coordinate and execute IRB-approved clinical trial activities including patient identification, screening, consent, enrollment, clinic visits, specimen collection (phlebotomy), ECGs, medication administration, regulatory compliance, eSource/data entry, AE/SAE tracking, and communication with PIs, sponsors, and monitors to ensure protocol adherence and efficient study conduct.

Lead and operate clinical research sites: oversee study setup and maintenance, screen and enroll patients, conduct clinic visits and direct patient care (consent, assessments, blood draws, ECG, med administration), ensure regulatory compliance and clean data, manage AE/SAE reporting, coordinate with PIs, sponsors, monitors, and drive site performance.

Coordinate and manage IRB-approved clinical trial activities including patient identification, screening, consenting, randomization, enrollment, clinic visits, specimen collection, medication administration, ECGs, regulatory compliance, clean data entry, adverse event tracking, and collaboration with PIs, sponsors, and monitors to ensure protocol adherence and quality patient care.

Enter and verify clinical trial data into EDC systems, review source documents, resolve data queries with study staff, maintain documentation and audit trails, ensure GCP/HIPAA compliance, and support monitoring, audits, and database lock timelines.

Coordinate and manage IRB‑approved clinical trials: identify, screen, randomize, enroll patients; conduct clinic visits and direct patient care (consent, assessments, blood draws, ECG, medication administration); ensure regulatory compliance, clean data entry, AE/SAE tracking, eSource maintenance; communicate with PIs, sponsors, and monitors; own assigned studies and patient care.

Coordinate and conduct IRB‑approved clinical trial activities including patient identification, screening, consenting, enrollment, clinic visits, specimen collection (phlebotomy), medication administration, ECGs, data entry, regulatory compliance, AE/SAE tracking, and communication with PIs, sponsors, and monitors.

Provide medical oversight as Sub-Investigator for clinical trials: ensure protocol compliance, perform exams and assessments, maintain subject safety, collaborate with site staff, attend sponsor meetings and audits, and uphold GCP/ICH/FDA standards.

Coordinate and conduct IRB‑approved clinical trial activities including patient identification, screening, consenting, enrollment, clinic visits, specimen collection (blood draws), ECGs, medication administration, data entry, regulatory compliance, and communication with PIs, sponsors, and monitors.

Coordinate IRB-approved clinical trial activities including patient identification, screening, consenting, enrollment, clinic visits, assessments, blood draws, ECG, medication administration, data entry, regulatory compliance, and communication with PIs, sponsors, and monitors.

Coordinate and execute IRB-approved clinical trial activities including patient identification, screening, consenting, enrollment, study visits, specimen collection (blood draws), ECGs, medication administration, regulatory documentation, data entry, AE/SAE tracking, and communication with PIs, sponsors, and monitors to ensure protocol compliance and quality.

Provide direct patient-facing support for IRB-approved clinical trials: recruit, screen, consent, enroll, conduct visits, perform phlebotomy/ECG/medication administration, maintain eSource and regulatory documentation, track adverse events, and communicate with investigators and sponsors.

Coordinate and conduct IRB‑approved clinical trial activities including screening, consenting, enrollment, clinic visits, phlebotomy, ECGs, medication administration, AE/SAE tracking, regulatory documentation, and data entry while supporting investigators, sponsors, and monitors.

Coordinate IRB-approved clinical trial activities including patient identification, screening, consenting, enrollment, clinic visits, specimen collection (phlebotomy), ECGs, medication administration, data entry, regulatory compliance, adverse event tracking, and communication with PIs, sponsors, and monitors.

Coordinate and manage IRB-approved clinical trial activities including patient identification, screening, consent, enrollment, clinic visits, data entry, regulatory compliance, AE/SAE tracking, and direct patient care procedures (blood draws, ECG, medication administration). Serve as liaison with PIs, sponsors, and monitors and ensure protocol adherence and clean study documentation.

Serve as Sub-Investigator for assigned clinical trials: provide medical oversight, perform and document exams and assessments, ensure protocol compliance and subject safety, collaborate with site staff and sponsors, and support monitoring, audits, and regulatory adherence (GCP/ICH/FDA).