Clinical Research Coordinator II - Hybrid Trials Specialist

Tufts Medicine; Lowell (MI); Hybrid; USD 48,000 - 60,000; Full time

Job summary

Tufts Medicine is seeking a Clinical Research Coordinator to assist the PI in planning and implementing clinical studies at Lowell General Hospital. You will recruit participants, obtain informed consent, coordinate visits, and ensure data quality and regulatory compliance.

The role emphasizes meticulous documentation, data entry, IRB submissions, adverse event reporting, and adherence to GCP guidelines. Strong organization and communication skills are essential; BLS may be required.

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.

Responsibilities

• Assist in recruitment of study participants and screening for eligibility.
• Obtain informed consent and coordinate protocol‑required visits.
• Complete data entry and case report forms with accuracy.
• Maintain regulatory binders, source documents, and study files.
• Assist with IRB submissions and adverse event reporting.

Skills

Organizational skills

Attention to detail

Computer skills

Prioritization

Communication

Record-keeping

Education

Bachelor’s degree

High School Diploma or equivalent

Job description

Tufts Medicine is seeking a Clinical Research Coordinator to assist the PI in planning and implementing clinical studies at Lowell General Hospital. You will recruit participants, obtain informed consent, coordinate visits, and ensure data quality and regulatory compliance.

The role emphasizes meticulous documentation, data entry, IRB submissions, adverse event reporting, and adherence to GCP guidelines. Strong organization and communication skills are essential; BLS may be required.