Research Study Coordinator
About The Position
The Research Study Coordinator is responsible for off-site study coordination and data management oversight for research protocols. The role works with investigators at BMC to develop case report forms consistent with clinical protocols, establish standard operating procedures for clinical conduct and data collection, assist site staff and investigators with study implementation, and conduct quality assurance audits to validate data before analysis by biostatisticians. The coordinator implements and monitors quality control procedures and conducts periodic quality assurance monitoring. The position coordinates protocol initiation and the establishment of operating policies and procedures; plans, implements, and maintains data collection and analysis systems; and supports research subjects, investigators, researchers, and technical support staff. It ensures the efficient day-to-day operation of research and data collection activities, monitors research progress, maintains activity records, and prepares reports as requested by investigators, administrators, funding agencies, or regulatory bodies. The coordinator also participates in ongoing clinical floor activities with research staff to ensure adequate clinical support for trial activities. This is a full-time position in the Research—Nephrology department.
Requirements
- Bachelor's degree required, preferably in Public Health.
- At least two years of experience with R statistical computing software.
- Understanding of data management in clinical research.
- Experience with clinical or epidemiologic research, especially in international health or chronic kidney disease.
Nice To Haves
- MS or MPH strongly preferred.
Responsibilities
- Coordinate research study protocol initiation and establish operating policies and procedures.
- Plan, implement, and maintain data collection and analysis systems; coordinate collection and analysis of research data as needed.
- Coordinate research subjects in accordance with study objectives and scope.
- Ensure efficient day-to-day operation of research and data collection activities and serve as the primary administrative contact for research subjects and principal investigators.
- Coordinate technical support staff engaged in research protocols and perform protocol-related work as required.
- Supervise and coordinate support services for investigators and researchers.
- Monitor research activities, maintain records, and prepare periodic and ad hoc reports for investigators, administrators, funding agencies, and regulatory bodies.
- Implement quality control processes throughout the trial and conduct quality assurance monitoring and audits to validate data.
- Work with investigators to develop case report forms and establish SOPs for clinical conduct and data collection.
- Assist site staff and investigators with study implementation and work with investigators at BMC.
- Participate in ongoing clinical floor activities with research staff to ensure adequate clinical support for trial activities.
- Perform miscellaneous job-related duties as assigned.
Benefits
- Medical, dental, vision, and pharmacy benefits.
- Discretionary annual bonuses and merit increases.
- Flexible Spending Accounts.
- 403(b) savings matches.
- Paid time off.
- Career advancement opportunities.
- Resources to support employee and family well-being.
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What This Job Offers
Job Type
Full-time
