Clinical Research Coordinator II - Trials & Impact

Tufts Medical Center, Inc.; Boston (MA); On-site; USD 48,000 - 60,000; Full time

Benefits offered by this job

Total Rewards package

Competitive base pay

Job summary

Tufts Medicine in the Boston area is seeking a clinical research assistant to support planning and execution of studies under the PI. You will recruit participants, manage data entry, and help ensure regulatory compliance across study documents.

The role emphasizes meticulous data handling, patient confidentiality, and coordination with lab and clinical teams. A background in research and familiarity with clinical trial processes are preferred.

Qualifications

• Minimum Qualifications: Bachelor’s degree OR High School Diploma or equivalent AND Four (4) years of related experience.
• Two (2) years in research related activities.
• Preferred Qualifications: Five (5) years in research related activities.
• Previous experience in clinical trials.
• IATA Hazardous Good Shipping certification.
• CITI Human Research Protection certification.

Responsibilities

• Assist in planning and implementing clinical research studies as assigned.
• Recruit study participants and screen for eligibility.
• Maintain regulatory binders and study documents.
• Coordinate data entry, data queries, and CRFs.
• Monitor adverse events and report to PI and IRB as required.
• Ensure HIPAA and FDA Good Clinical Practice compliance.

Skills

Organizational skills

Data collection & analysis

Communication skills

Computer skills

BLS certification

Education

Bachelor’s degree or high school diploma with 4 years experience

Tools

Microsoft Office

Electronic data capture (EDC) systems

Job description

Tufts Medicine in the Boston area is seeking a clinical research assistant to support planning and execution of studies under the PI. You will recruit participants, manage data entry, and help ensure regulatory compliance across study documents.

The role emphasizes meticulous data handling, patient confidentiality, and coordination with lab and clinical teams. A background in research and familiarity with clinical trial processes are preferred.