Jobs at ObjectiveHealth

Coordinates clinical trials across gastroenterology, urology, dermatology, and oncology studies. Responsibilities include patient identification, screening, consent, enrollment, randomization, clinic visits, direct patient care, blood draws, medication administration, ECGs, data entry, regulatory compliance, IRB responses, adverse event tracking, study setup, and communication with investigators, sponsors, and monitors.

Coordinates clinical research studies and patient activities, including participant identification, screening, enrollment, consent, assessments, blood draws, medication administration, ECGs, data entry, regulatory compliance, IRB responses, adverse-event tracking, and study maintenance. The role requires collaboration with investigators, sponsors, monitors, and research teams while following approved protocols and supporting trials in multiple therapeutic areas. Spanish bilingual communication and direct patient-care skills are important.

Coordinates clinical research protocols from patient identification and screening through enrollment, visits, data entry, regulatory compliance, and study maintenance. Performs or assists with patient care activities including informed consent, physical assessments, blood draws, medication administration, and ECGs. Manages multiple studies, IRB responses, audit findings, adverse events, source documentation, and communication with investigators, sponsors, monitors, and research teams.

Conduct clinical research protocols from patient identification, screening, randomization, and enrollment through clinic visits and study maintenance. Perform or assist with patient care activities including informed consent, physical assessments, blood draws, medication administration, and ECGs. Maintain accurate data, regulatory compliance, IRB responses, audit findings, adverse event tracking, and eSource records while coordinating with research teams, investigators, sponsors, and monitors.

Conduct clinical research protocols from patient identification, screening, randomization, and enrollment through clinic visits and study maintenance. Perform direct patient care activities including informed consent, physical assessments, blood draws, medication administration, and ECGs. Maintain accurate data, regulatory compliance, IRB responses, audit findings, adverse event tracking, and eSource documentation while coordinating with investigators, sponsors, monitors, and research teams.

Supports clinical research studies through patient interaction, vitals, physical assessments, blood draws, medication administration, ECGs, data entry, regulatory compliance, protocol adherence, study maintenance, and communication with research teams, investigators, sponsors, and monitors.

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.

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 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.