Role Summary
We are seeking a skilled and detail-oriented professional to support our clinical research operations.
This role is responsible for coordinating clinical trials, ensuring study protocols are followed, and maintaining accurate records. The ideal candidate will have strong communication skills, the ability to work independently, and a passion for delivering high-quality results.
Responsibilities:
* Develop a deep understanding of assigned studies through protocol review, investigator meetings, and coordination with Principal Investigators
* Ensure strict adherence to study protocols, obtaining exemptions when necessary/appropriate
* Communicate protocol issues to relevant stakeholders, including CROs, Sponsors, Site Administrators, Directors, and Investigators
* Collect and maintain initial psychiatric and medical information from patients, accessing other relevant sources as needed
* Maintain effective communication channels between patients, study staff, referral sources, Sponsors, and monitoring teams
* Accurately document source data and sponsor-required information in a timely manner
* Dispense and track study medication, maintaining accurate records
* Educate patients and families about their specific study and clinical drug trials in general
* Address monitor and sponsor queries in a prompt and efficient manner
Requirements:
* Bachelor's degree or higher; related field preferred
* Minimum two years of experience in a clinical environment; clinical research experience an asset
* LPN, RN, or other medical licensure/certification required
* BLS Healthcare Provider certification mandatory
* Bilingual Spanish-English proficiency a plus
About Us:
We prioritize people and seek individuals who excel at building relationships, empathize with patients and staff, and embody a patient-first approach. We value diversity and individuality, promoting a culture of humility and respect.