Temporary Patient Care Coordinator

Axle•Rockville, MD

3d•Hybrid

About The Position

Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH). Axle is seeking a Temporary Patient Care Coordinator to join our vibrant team at the National Institutes of Health (NIH) supporting the Bethesda, MD.

Requirements

Associate's degree required.
Minimum of 4 years of related experience.
Strong written and verbal communication skills.
Strong patient-facing and customer-service abilities.
Ability to coordinate multiple schedules, priorities, and clinical activities simultaneously.
Strong organizational skills and attention to detail.
Ability to work effectively with physicians, investigators, clinical staff, patients, and families.
Proficiency with Microsoft Office Suite, including spreadsheet and calendar management.

Nice To Haves

Bachelor's degree in a related discipline preferred.
Preferred field of study: Health and Medical Administrative Services.

Responsibilities

Coordinate the recruitment, scheduling, travel, lodging, and admission of research study participants.
Serve as a primary point of contact for patients participating in clinical research studies.
Coordinate patient schedules with physicians, nurses, investigators, clinical research coordinators, testing personnel, and outpatient clinic staff.
Schedule new patient screening appointments, procedures, imaging studies, outpatient visits, and inpatient admissions.
Maintain calendars and shared calendars for clinical staff and research activities.
Maintain the Reproductive Endocrinology patient calendar, including incoming and departing patients, clinic support, and pre- and post-examination coordination.
Send appointment reminders and follow up with patients regarding scheduled visits.
Coordinate patient travel and lodging and maintain related travel documentation.
Assist with chart preparation for surgeries and post-operative admissions.
Request interpreter services for returning patients when needed.
Support clinical studies involving subject enrollment, longitudinal monitoring, study data, sample collection, consent-related coordination, and data entry.
Maintain ongoing communication with patients, families, caregivers, healthcare providers, investigators, and research staff.
Respond to patient phone calls and emails and appropriately prioritize urgent, emergent, and routine issues.
Triage patient questions and concerns to the appropriate clinical or research team member.
Explain relevant study policies and procedures to research participants.
Serve as a point of contact for patient questions regarding research protocols.
Communicate protocol information to patients within the context of applicable eligibility requirements.
Prepare correspondence requiring an understanding of clinical or technical program information.
Review incoming patient referrals and ensure required information is complete.
Contact referring physicians' offices when additional documentation is needed.
Coordinate referral materials and submissions with appropriate clinical staff.
Refer prospective study volunteers to appropriate Institute personnel in accordance with study guidelines.
Maintain clinical information within protocol databases.
Create and format spreadsheets used to organize and analyze information.
Support the conversion and organization of paper records into electronic files.
Maintain participant confidentiality and support the safety and privacy of research participants.
Maintain office and clinical research records.
Assist with procurement and reimbursement-related processes.
Coordinate meetings, appointments, conference rooms, workshops, and other scheduling needs.
Prepare and maintain reports, forms, memoranda, mailings, spreadsheets, and administrative databases associated with clinical research operations.