Clinical Research Coordinator II — Study Operations

Tufts Medicine; Boston (MA); On-site; USD 48,000 - 60,000; Full time

Job summary

Tufts Medicine is seeking support for planning and implementing clinical research studies under the supervision of the Principal Investigator. The role involves coordinating recruitment, data collection, and regulatory compliance to advance research projects and clinical trials.

Ideal candidates will have a background in biosciences, at least two years in research, and familiarity with IRB processes. The position emphasizes meticulous data management, patient confidentiality, and adherence to

Qualifications

• Bachelor’s degree OR High School Diploma or equivalent AND Four (4) years of related experience.
• Basic Life Support (BLS) certification may be required based on specific role requirements.
• Two (2) years in research related activities.
• Five (5) years in research related activities.
• Previous experience in clinical trials.
• IATA Hazardous Good Shipping certification.
• CITI Human Research Protection certification.

Responsibilities

• Assist recruitment of study participants and screen for eligibility.
• Complete follow-up with study participants in prescribed settings.
• Complete data abstraction of source documents and CRFs per best practices.
• Ensure compliance with human subjects protections and IRB requirements.
• Coordinate tests and procedures per protocol requirements and report results.
• Maintain study documents, regulatory binders, and inventory of study supplies.

Skills

BLS certification

Education

Bachelor’s degree

High School Diploma

Job description

Tufts Medicine is seeking support for planning and implementing clinical research studies under the supervision of the Principal Investigator. The role involves coordinating recruitment, data collection, and regulatory compliance to advance research projects and clinical trials.

Ideal candidates will have a background in biosciences, at least two years in research, and familiarity with IRB processes. The position emphasizes meticulous data management, patient confidentiality, and adherence to