Research Study Coordinator
- Pay
- $20 – $29 per hour
- Location
- Boston, MA · On-site
- Job type
- Full-time
- Level
- Mid-level
- Experience
- 2+ years
- Listed
- 21 days ago
Skills & highlights for this role
- clinical research data management
- R statistical software
- clinical study protocol implementation
Also useful
- case report form development
- quality assurance auditing
Stated benefits & perks
- Medical
- Dental
- Vision
Position Summary
The Research Study Coordinator is responsible for off-site study coordination and data management oversight. The Study Coordinator will provide study coordination of specific protocols - including implementing and monitoring quality control SOPs; conducting period quality assurance monitoring; and working with investigators at BMC.
The Study Coordinator will work with investigators to develop case report forms consistent with clinical protocols, sets up SOPs for clinical conduct, data collection, assist site staff/investigators in study implementation and performs quality assurance audits to validate data in preparation for analysis by biostatisticians.
Position: Research Study Coordinator Department: Research.- Nephrology Schedule: Full Time ESSENTIAL DUTIES & RESPONSIBILITIES: Coordinates the initiation of research study protocol, and the establishment of operating policies and procedures. Plans, implements, and maintains data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data.
Coordinates research subjects as appropriate to specific study objectives and work scope. Ensures the smooth and efficient day-to-day operation of research and data collection activities; acts as the primary administrative point of contact for research subjects and principal investigators.
Coordinates the day-to-day activities of any technical support staff specifically engaged in the carrying out of research protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives. Supervises and coordinates the provision of support services to investigators and researchers.
Monitors the progress of research activities; develops and maintains records of research activities, and prepares periodic and ad hoc reports, as required by investigators, administrators, funding agencies, and/or regulatory bodies. To implement quality control process throughout the conduct of the trial.
To participate in clinical floor activities on an ongoing basis with research staff to ensure adequate clinical support for trial activities. To perform miscellaneous job-related duties as assigned. JOB REQUIREMENTS EDUCATION: Bachelors' degree required, preferably in Public Health. Preferred Education and Experience: MS/MPH strongly preferred.
EXPERIENCE: Must have minimum of two (2) years experience with R statistical computing software, understanding of data management in clinical research and experience with clinical/epidemiologic research, especially in international health / Chronic kidney disease Compensation Range: $20.43- $28.61 This range offers an estimate based on the minimum job qualifications.
However, our approach to determining base pay is comprehensive, and a broad range of factors is considered when making an offer. This includes education, experience, skills, and certifications/licensures as they directly relate to position requirements; as well as business/organizational needs, internal equity, and market-competitiveness.
In addition, BMCHS offers generous total compensation that includes, but is not limited to, benefits (medical, dental, vision, pharmacy), discretionary annual bonuses and merit increases, Flexible Spending Accounts, 403(b) savings matches, paid time off, career advancement opportunities, and resources to support employee and family well-being.
NOTE: This range is based on Boston-area data, and is subject to modification based on geographic location. Our current job openings are listed on our website and applications are received only through our website. We do not ask or require downloads of any applications, or "apps" job offers are not extended over text messages or social media platforms. We do not ask individuals to purchase equipment for or prior to employment.
Equal opportunity and legal notices
Equal Opportunity Employer/Disabled/Veterans According to the FTC, there has been a rise in employment offer scams.
From BMC's careers page, first listed on Rolev.ai on October 19, 2026. Rolev.ai is not the employer.
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Common questions
What is the salary for the Research Study Coordinator role at BMC?
The Research Study Coordinator posting at BMC states compensation of $20 – $29 per hour. It is listed as a full-time position. Final pay may depend on location, experience, and interview evaluation on BMC's official career site.
Where is the Research Study Coordinator job at BMC located?
This Research Study Coordinator position at BMC is located in Boston, MA (On-site). Always check BMC's application page for specific state eligibility or relocation policies.
What qualifications are required for Research Study Coordinator at BMC?
For the Research Study Coordinator role, BMC highlights 2+ years of relevant experience; experience with clinical research data management, R statistical software, clinical study protocol implementation. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.
How do I apply for the Research Study Coordinator position at BMC?
This listing links directly to BMC's Workday application page. You can apply directly on BMC's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.