Research Study Coordinator
About The Position
The Research Study Coordinator is responsible for off-site study coordination and data management oversight for specific 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, and assist site staff and investigators with study implementation. The coordinator implements and monitors quality control procedures, conducts periodic quality assurance monitoring and audits to validate data, and prepares data for analysis by biostatisticians. The position coordinates protocol initiation and operating procedures; plans and maintains data collection and analysis systems; coordinates research subjects and research activities; and supports the day-to-day operation of research and data collection. It also coordinates technical support staff as appropriate, provides support services to investigators and researchers, monitors research progress, maintains activity records, and prepares reports. The coordinator participates in 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. The listed compensation range is $20.43–$28.61; the posting notes that the range is an estimate based on minimum qualifications, is based on Boston-area data, and may be modified based on geographic location. BMCHS also describes benefits and other components of total compensation.
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.
Nice To Haves
- Master’s degree or MPH strongly preferred.
- Experience in international health and/or chronic kidney disease research preferred.
Responsibilities
- Coordinate initiation of research study protocols and establish operating policies and procedures.
- Plan, implement, and maintain data collection and analysis systems in support of research protocols; may coordinate collection and analysis of research data.
- Coordinate research subjects as appropriate to study objectives and work scope.
- Ensure smooth day-to-day operation of research and data collection activities and serve as the primary administrative point of contact for research subjects and principal investigators.
- Coordinate day-to-day activities of technical support staff engaged in research protocols, as appropriate, and perform aspects of protocols 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 as required.
- Implement quality control processes throughout clinical trials.
- Participate in clinical floor activities with research staff to ensure adequate clinical support for trial activities.
- Assist investigators with developing case report forms consistent with clinical protocols.
- Establish SOPs for clinical conduct and data collection and assist site staff and investigators with study implementation.
- Conduct periodic quality assurance monitoring and audits to validate data in preparation for biostatistical analysis.
- 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
Career Level
Mid Level
