Clinical Research Coordinator - Project Hire

Responsibilities Adhere to the IRB‑approved protocol and coordinate protocol‑related research procedures, study visits, and follow‑up care, ensuring accurate execution of research protocols in accordance with Good Clinical Practices, HIPAA, and all required obligations to patient/subject, Principal Investigator, Research Team, sponsor, and other appropriate agencies. Act as an active participant in all study components from research planning to study completion, including direct involvement in case management of study participants, study coordination, and data collection to ensure compliance in study conduct and adherence to the study protocol. Participate in pre‑screening and recruitment activities to identify patients who may be eligible for research study participation. Run participants through experiments and record study data per the clinical study protocol. Ensure the participant has a positive experience and that high‑quality data is collected. Share feedback from participants to help improve the participant experience. Function as liaison between research sites, clinicians, participants, and other internal and external stakeholders. Maintain accurate data records and a follow‑up calendar, ensuring all follow‑up assessments are completed per protocol. Own study progress and updates in team project management software. Proactively alert the study manager and study team of issues that may arise. Manage and respond to project‑related email and phone inquiries. Maintain effective communication with research participants when engaging in participant recruitment, enrollment, tracking, retention, and data collection. Enter data (e.g., transfer study data from paper forms to the electronic database). Prepare, maintain, and update technical documentation. Attend weekly project meetings. Coordinate with the research team, clinicians, and engineering to ensure project success. Perform any other duties needed to help drive the company’s vision, fulfill its mission, and abide by its values. Qualifications (No specific degree required; familiarity with research studies and tabular data is preferred.) Excellent attention to detail. Strong interest in clinical research. Prior laboratory or human subjects research experience. Professional demeanor, especially when interacting with participants. Strong organizational and interpersonal skills. Benefits & Work Arrangements The anticipated duration of the position is 6–12 months, not initially eligible for company‑sponsored benefits. If the position extends beyond one year, benefit eligibility will be determined in accordance with the Company’s benefit plans and eligibility requirements in effect at that time. Hybrid work schedule: employees are expected to work in the office regularly and may work remotely as approved by a manager and based on business needs. Commuter benefits for parking, public transit, carshares, etc. Fully stocked kitchen. #J-18808-Ljbffr Senseye, Inc.