Jobs at ObjectiveHealth

Serve as Sub-Investigator for assigned clinical trials, ensuring protocol compliance and subject safety. Perform and document physical exams and medical assessments, provide medical oversight throughout trial phases, collaborate with site staff and sponsors, participate in monitoring and audits, and maintain adherence to GCP, ICH, FDA regulations and internal SOPs.

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.

Lead and operate a clinical research site: coordinate industry-sponsored trials, enroll and care for patients, perform consenting and clinical procedures, ensure data quality and regulatory compliance, track AEs/SAEs, manage study setup and maintenance, liaise with PIs, sponsors, and monitors, and mentor site staff to meet enrollment and protocol goals.

Coordinate IRB-approved clinical trial activities including patient identification, screening, consent, enrollment, clinic visits, phlebotomy, ECGs, medication administration, data entry, regulatory compliance, AE/SAE tracking, and communication with PIs, sponsors, and monitors.

Coordinate and manage IRB-approved clinical trials: screen, consent, enroll patients; perform direct patient care (assessments, blood draws, ECGs, med administration); ensure regulatory compliance, clean data entry, AE/SAE tracking, and communication with PIs, sponsors, and monitors. Support study set-up, maintenance, and audit readiness in gastroenterology, urology, dermatology, or oncology trials.

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.

Perform direct patient-facing clinical research tasks including phlebotomy/vitals, assist with physical assessments, ECGs, medication administration, accurate data entry, regulatory compliance, study setup/maintenance, and coordination with investigators and sponsors.

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).