Clinical Research Coordinator II: Trials, IRB & Compliance

Tufts Medicine; Lowell, Northern (MA, KY); Hybrid; USD 65,000 - 90,000; Full time

Job summary

Tufts Medicine is seeking a Clinical Research professional to support the development of new products and the innovation of clinical trial processes within our research programs.

You will assist the Principal Investigator in planning and implementing clinical studies, coordinating IRB submissions, ensuring HIPAA compliance, and reporting results in line with FDA Good Clinical Practice guidelines, under close supervision.

Qualifications

• Bachelor's degree OR High School Diploma or equivalent AND four years of related experience.
• Basic Life Support (BLS) certification may be required based on role requirements.
• Preferred qualifications include experience in clinical trials.

Responsibilities

• Assist with IRB requirements for each study including education, submissions, adverse event reporting and annual reviews.
• Maintain patient confidentiality per HIPAA and ensure study information is secure.
• Adhere to FDA Good Clinical Practice Guidelines and coordinate tests per protocol.

Skills

Organizational skills

Data collection & analysis

Excellent communication

Education

Bachelor's degree

High School Diploma or equivalent

Job description

Tufts Medicine is seeking a Clinical Research professional to support the development of new products and the innovation of clinical trial processes within our research programs.

You will assist the Principal Investigator in planning and implementing clinical studies, coordinating IRB submissions, ensuring HIPAA compliance, and reporting results in line with FDA Good Clinical Practice guidelines, under close supervision.