Jobs at ObjectiveHealth

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 and manage IRB-approved clinical trials: identify, screen, randomize, and enroll patients; conduct clinic visits; consent and perform assessments (blood draws, ECG, medication administration); ensure data quality, regulatory compliance, AE/SAE tracking, and clear communication with PIs, sponsors, and monitors.

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.

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 screening, consenting, enrollment, clinic visits, phlebotomy, ECGs, medication administration, AE/SAE tracking, regulatory documentation, and data entry while supporting investigators, sponsors, and monitors.

Lead and manage clinical research site operations, oversee protocol execution and patient enrollment, perform patient-facing clinical tasks (consent, assessments, blood draws, ECG), ensure regulatory compliance and clean data entry, track AEs/SAEs, liaise with PIs, sponsors, and monitors, and maintain study documentation and eSource.

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.

Part-time NP/PA serves as Sub-Investigator overseeing assigned clinical trials, ensuring protocol compliance, participant safety, conducting medical assessments, collaborating with site staff, participating in sponsor and monitoring visits, and maintaining GCP/ICH/FDA regulatory standards.

Serve as part-time Principal Investigator overseeing clinical trials: ensure protocol compliance and subject safety, perform medical assessments, provide ongoing medical oversight, collaborate with site staff, participate in sponsor meetings, and maintain compliance with GCP/ICH/FDA and internal SOPs.

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

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

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