Clinical Research Coordinator: Study Operations & IRB Support

Tufts Medical Center, Inc.; United States; On-site; USD 45,000 - 56,000; Full time

Job summary

Tufts Medicine is seeking an entry to mid-level Clinical Research Support role to assist the Principal Investigator in planning and implementing clinical studies. The position involves participant recruitment, data collection, and coordination of regulatory activities, with emphasis on protocol adherence and patient confidentiality.

Opportunities to engage in site visits and data quality checks exist within a clinical research setting.

Qualifications

• Bachelor’s degree or equivalent with 4 years of related experience.
• BLS certification may be required depending on role requirements.
• Two years in research related activities preferred.
• IATA Hazardous Goods Shipping certification preferred.
• CITI Human Research Protection certification preferred.

Responsibilities

• Assists in recruitment of study participants.
• Completes follow-up with study participants as required.
• Performs data collection, abstraction, and source document review per protocol.
• Ensures compliance with regulatory requirements and HIPAA guidelines.
• Supports IRB submissions and annual reviews as needed.
• May perform basic laboratory activities as required.
• Maintains study documents and inventory of supplies.

Skills

Organizational skills

Data collection & analysis

Attention to detail

Computer skills

Prioritization

Communication & interpersonal skills

Record-keeping

Education

Bachelor’s degree or equivalent + 4 years experience

BLS certification

IATA Hazardous Goods Shipping certification

CITI Human Research Protection certification

Job description

Tufts Medicine is seeking an entry to mid-level Clinical Research Support role to assist the Principal Investigator in planning and implementing clinical studies. The position involves participant recruitment, data collection, and coordination of regulatory activities, with emphasis on protocol adherence and patient confidentiality.

Opportunities to engage in site visits and data quality checks exist within a clinical research setting.