Clinical Research Coordinator - Trials & IRB Specialist

Tufts Medicine

Boston (MA)

On-site

USD 45,000 - 56,000

Full time

5 days ago
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Job summary

Tufts Medical Center in Boston is seeking a Clinical Research Coordinator to assist the Principal Investigator in planning and implementing clinical studies, manage data collection, regulatory documents, and participant recruitment. You will liaise with teams to ensure protocol adherence and timely study progress.

Strong organizational skills, meticulous attention to detail, and proficiency with data entry and regulatory processes are essential.

Qualifications

  • Bachelor’s degree or high school diploma plus four years related experience.
  • BLS certification may be required depending on role.
  • Two years in research activities preferred.
  • IATA Hazardous Goods Shipping certification preferred.
  • CITI Human Research Protection certification preferred.

Responsibilities

  • Assist in recruitment of study participants and follow-ups.
  • Complete source document abstraction and CRF completion.
  • Ensure compliance with IRB, FDA GCP, and HIPAA requirements.
  • Maintain regulatory binders, study materials, and inventory.
  • Coordinate tests, reports, and data queries; enter data as warranted.
  • Participate in site visits and maintain clear communication with sponsor.

Skills

Organization and data collection
Attention to detail
Excellent computer skills
Prioritize quickly
Communication and interpersonal skills
Systematic record-keeping
Regulatory documentation management

Education

Bachelor’s degree
High School Diploma or equivalent

Job description

Tufts Medical Center in Boston is seeking a Clinical Research Coordinator to assist the Principal Investigator in planning and implementing clinical studies, manage data collection, regulatory documents, and participant recruitment. You will liaise with teams to ensure protocol adherence and timely study progress.

Strong organizational skills, meticulous attention to detail, and proficiency with data entry and regulatory processes are essential.

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