Note: The job is a remote job and is open to candidates in USA. The University of Pittsburgh Department of Medicine’s Renal-Electrolyte Division is seeking a temporary Renal Clinical Research Coordinator to support multiple nephrology research studies. The role involves participant recruitment, eligibility screening, and maintaining study data, while ensuring compliance with research protocols.
Responsibilities
- Participant recruitment
- Eligibility screening
- Obtaining informed consent
- Recruit and schedule patients and healthcare providers for research interviews
- Maintain recruitment tracking records
- Coordinate baseline assessments and follow-up study visits
- Enter and maintain study data in REDCap
- Process Vincent study participant payments
- Prepare materials for study recruitment campaigns
- Participate in community outreach meetings
- Assist with the preparation of study reports
- Ensure that study activities are completed in accordance with approved protocols, manuals of procedures, and established study workflows
- Maintain professional and collaborative relationships with community partners, including chronic kidney disease and dialysis clinic staff, healthcare providers, patients, and other study stakeholders
Skills
- Excellent written and verbal communication skills
- Organizational skills
- Time-management skills
- Ability to communicate professionally with research participants, healthcare providers, clinic staff, community partners, and other study stakeholders
- Ability to manage responsibilities across multiple research studies
- Ability to maintain accurate and confidential study records
- Ability to follow detailed research protocols and established workflows
- Ability to prioritize tasks based on study needs and deadlines
- Attention to detail
- Reliability
- Professionalism
- Ability to work both independently and collaboratively
- Comfortable conducting telephone and in-person participant interactions
- Ability to work primarily in a remote environment
- Ability to maintain a flexible work schedule based on study activities
- Willingness to travel to local chronic kidney disease and dialysis clinics approximately two to three times per month
- Experience with participant recruitment, eligibility screening, informed consent, clinical research coordination, data collection, or research data entry
- Experience using REDCap or a similar research data management system
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