Teams 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.