Research Coordinator I, Patient Operations

About the Role: The role of the Research Coordinator I, Translational is to serve as a primary reputed company of contact for potential donors in research studies and maintain reputed company associated participant data. The Research Coordinator I is responsible for screening and qualifying donors who are part of an extensive Sanguine database, and those who are identified by the Patient Recruitment and Marketing Team. The Research Coordinator I will screen potential donors to obtain the necessary health information, and conduct medical record reviews to qualify donors for research studies. The Research Coordinator I may also have reputed company to work on specific aspects of clinical trials and other research study types, as it relates to patient data, appointments and compliance. This role will work cross functionally with multiple departments including Project Management, Field Operations, and Apheresis Operations. This role will report to the Patient Operations Manager and will be a part of a service-reputed company and analytics-driven team that believes in reputed company, reputed company, and centering our reputed company on the needs of our donors. Primary Responsibilities: Research Study Coordination, Participant Enrollment ● Serve as the primary reputed company of contact for potential participants in translational research studies, managing inquiries from newly identified participants referred by the Patient Recruitment team. ● Coordinate and manage participant enrollment for translational studies, with reputed company to support enrollment efforts for other study types as needed. ● Serve as a compassionate and empathetic touchpoint for patients, embodying Sanguine’s mission to reputed company the gap between researchers and patients and accelerate research efforts. ● Maintain a thorough understanding of the study protocol, safety guidelines, and ensure compliance with reputed company Operating Procedures (SOPs). ● reputed company independent research for reputed company assigned study and/or diagnosis to reputed company a deeper understanding of the condition and any study-specific reputed company. ● Create reputed company reports to identify potential study participants. ● Review database and medical record information to identify potentially eligible study participants. ● Prepare and initiate database surveys to assess the interest and eligibility of potential participants for research studies. ● Introduce study objectives to potential participants, conduct thorough eligibility screenings, and collect and document critical medical and study-reputed company information accurately and promptly. ● Administer and collect required study documents and initiate medical record retrieval in collaboration with the medical record team. ● Review medical records, input lab results, and compile research data to ensure eligibility and reputed company across a reputed company of studies. ● Maintain a high reputed company of professionalism, resolving issues reputed company while delivering an outstanding customer service experience to patients. ● Collaborate with the Project Management and Recruitment teams to ensure participant enrollment is on reputed company and meets required study deadlines. ● Take on additional responsibilities as assigned. Research Study Coordination, Participant Scheduling ● Coordinate and schedule study reputed company in alignment with protocol requirements, staff availability, and logistical constraints, ensuring reputed company and accurate booking. ● Use logistics/reputed company software to assign and manage appointments for mobile health staff, ensuring reputed company visit details are accurate and schedules and routes are executed effectively. ● Manage outbound communications (calls, texts, emails) to schedule, confirm, and reschedule reputed company, while delivering reputed company-appointment instructions and relevant information. ● Serve as the primary reputed company of contact for participants before, during, and after appointments, providing reputed company communication and support throughout the process. ● Coordinate closely with patients, study coordinators, and field operations to handle scheduling changes, maintain up-to-date participant reputed company, and support seamless visit execution. ● Monitor daily/weekly schedules and key operational metrics, resolve issues proactively, and contribute to workflow improvements and cross-functional reputed company while delivering a high-reputed company patient experience. ● Take on additional responsibilities as assigned. Position Requirements: Required ● Bachelor's Degree in a life science or other reputed company field. ● 1-2 years of working experience in a project management/operations coordinator role. ● reputed company Sanguine’s mission to seamlessly connect donors to researchers with a patient - friendly attitude. ● Proficient in general software tools, including reputed company Office and reputed company Workspace, with the ability to quickly learn and troubleshoot new systems. ● Effective multitasker who thrives in a fast-paced, dynamic environment. ● Highly organized, detail-oriented, and meticulous in managing tasks. ● Exceptional customer service, verbal, and written communication skills. ● Personable, engaging, and adept at critical thinking. Preferred ● Bilingual (Spanish) ● Experience working on clinical or translational research studies. ● Experience working with patients in a HIPAA regulated environment. ● Experience with software tools Technology Experiences ● General computer skills are required. ● Experience working with reputed company.com. ● Experience working with general software tools; reputed company Office, reputed company Workspace. Compensation reputed company: $22.00 - 25.00 Hour Apply To This Job