Clinical Research Coordinator II: Drive Clinical Trials

Tufts Medical Center, Inc.; Boston (MA); On-site; USD 48,000 - 60,000; Full time

Job summary

Tufts Medical Center, Inc. is seeking a clinical researcher assistant to support planning and implementation of clinical studies under the Principal Investigator.

Responsibilities include recruitment, eligibility screening, data collection, IRB coordination, and regulatory documentation. The role demands strong organizational and communication skills, attention to detail, and the ability to work in a clinical/administrative setting.

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 (preferred).
• Previous experience in clinical trials (preferred).
• IATA Hazardous Good Shipping certification (preferred).
• CITI Human Research Protection certification (preferred).

Responsibilities

• Assist in recruitment of study participants.
• Screen study participants for eligibility.
• Complete follow up with study participants.
• Record abstraction of source documents and case report forms.
• Comply with policies and government regulations for human subjects’ protections.
• Assist with IRB requirements and educational requirements.
• Perform basic laboratory activities as needed.
• Maintain HIPAA confidentiality and FDA Good Clinical Practice guidelines.
• Identify and resolve protocol non-compliance issues.
• Arrange tests and procedures per protocol requirements.
• Conduct tests as appropriate (e.g., EKGs).
• Coordinate site visits with study sponsor.
• Maintain inventory of study supplies.
• Assess potential patients and eligibility for protocols.
• Review eligibility criteria in patient records.
• Obtain informed consent signatures.
• QC checks of CRFs prior to data entry.
• Resolve data queries and perform data entry.
• Maintain regulatory binders and study documents.
• Monitor adverse events and report to PI and sponsor.

Skills

Organizational skills

Data analysis

Attention to detail

Communication skills

Time management

Education

Bachelor's degree

High School Diploma + 4 years related experience

Tools

Microsoft Excel

Data management systems

Job description

Tufts Medical Center, Inc. is seeking a clinical researcher assistant to support planning and implementation of clinical studies under the Principal Investigator.

Responsibilities include recruitment, eligibility screening, data collection, IRB coordination, and regulatory documentation. The role demands strong organizational and communication skills, attention to detail, and the ability to work in a clinical/administrative setting.