Clinical Research Study Coordinator - Data & QA Lead

BMC Software; Boston (MA); On-site; USD 28,000 - 39,000; Full time

Job summary

BMC Software is seeking a Research Study Coordinator to manage off-site study coordination and data governance. You will implement SOPs, monitor quality control processes, and collaborate with investigators to develop CRFs aligned with clinical protocols.

You will oversee data collection activities, supervise staff, and ensure quality assurance audits support analysis by biostatisticians. This role emphasizes ongoing clinical support and adherence to protocol requirements.

Qualifications

• Bachelor's degree required, preferably in Public Health.
• MS/MPH strongly preferred.

Responsibilities

• Initiate research study protocols and establish operating policies.
• Plan and maintain data collection and analysis systems for the protocol.
• Coordinate research subjects per study objectives and scope.
• Serve as primary contact for research subjects and investigators.
• Oversee technical support staff involved in the protocol implementation.
• Supervise support services for investigators and researchers.
• Track progress and prepare reports for investigators and regulators.

Skills

R

Data management

Clinical research coordination

Quality control

Education

Bachelor's degree

MS/MPH preferred

Job description

BMC Software is seeking a Research Study Coordinator to manage off-site study coordination and data governance. You will implement SOPs, monitor quality control processes, and collaborate with investigators to develop CRFs aligned with clinical protocols.

You will oversee data collection activities, supervise staff, and ensure quality assurance audits support analysis by biostatisticians. This role emphasizes ongoing clinical support and adherence to protocol requirements.