Jobs at ObjectiveHealth

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.

Conduct clinical research protocols from patient identification, screening, randomization, and enrollment through clinic visits and study maintenance. Perform consenting, physical assessments, blood draws, medication administration, and ECGs. Maintain accurate data, eSource materials, regulatory documentation, adverse event tracking, and protocol compliance while coordinating with investigators, sponsors, monitors, and research teams.

Accurately enter, review, and maintain clinical trial data in EDC systems; verify and resolve data queries by comparing source documents; communicate with study staff; maintain documentation and audit trails; ensure compliance with study protocols, GCP, HIPAA, and regulatory requirements; support monitoring, audits, and database lock timelines.

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.

Coordinates clinical research studies and patient visits, including screening, enrollment, informed consent, assessments, blood draws, medication administration, ECGs, data entry, regulatory compliance, IRB responses, adverse-event tracking, and study maintenance. Requires strong patient-care skills, communication, attention to detail, and strict protocol adherence. Spanish bilingual ability and U.S. work authorization are required.

Conduct and coordinate IRB-approved clinical trials, including patient identification, screening, consent, enrollment, clinic visits, assessments, blood draws, medication administration, ECGs, data entry, regulatory compliance, adverse event tracking, IRB responses, audit findings, and eSource maintenance. Build effective relationships with research teams, investigators, sponsors, and monitors while ensuring protocol adherence and patient-focused care.

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).

Supports clinical research studies by interacting directly with patients, taking vitals, performing or assisting with assessments, blood draws, medication administration, and ECGs. Maintains accurate data entry, patient reports, eSource materials, regulatory compliance, lab cleanliness, study documentation, and protocol adherence. Collaborates with research staff, principal investigators, sponsors, and monitors while supporting study setup, maintenance, and patient enrollment.

Coordinate and manage IRB‑approved clinical trial activities including patient identification, screening, consenting, enrollment, clinic visits, assessments, blood draws, ECGs, medication administration, data entry, regulatory compliance, AE/SAE tracking, and eSource maintenance. Serve as primary liaison with PIs, sponsors, and monitors while ensuring protocol adherence and high-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 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.

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 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 IRB-approved clinical trials: identify, screen, randomize, and enroll patients; perform consenting, assessments, blood draws, medication administration, and ECGs; ensure clean data entry, regulatory compliance, AE/SAE tracking, eSource maintenance, and communication with PIs, 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.

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.

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.