Part-Time Cardiology Clinical Research Assistant

Boston Children’s Hospital; Boston (MA); On-site; USD 28,000 - 41,000; Part time

Benefits offered by this job

Flexible schedules

Health insurance

Vision and dental insurance

Student loan subsidies

Time off

Tuition reimbursement

License reimbursement

Discounted commuter benefits

Job summary

Boston Children’s Hospital’s Cardiovascular, Critical Care and Perioperative, Patient Services team is seeking a Part-Time Clinical Research Assistant (Nursing Research). You will support nurse-led projects, coordinate trials, and work with investigators and clinical teams to ensure studies meet standards and procedures.

Responsibilities include IRB submissions, patient enrollment, REDCap data entry, data quality checks, and contributing to abstracts and posters.

Qualifications

• Bachelor's degree in STEM or Psychology is required.
• 0-1 years of relevant research experience is preferred.
• Familiarity with IRB processes is preferred.
• Experience with REDCap preferred.

Responsibilities

• Assist with managing regulatory activities for new and ongoing clinical trials, including IRB submissions, amendments, continuing reviews, and maintenance of study files.
• Obtains informed consent and enrolls patients in research studies. Reviews clinical information to identify patients meeting study inclusion criteria.
• Serves as liaison to participants in the research studies.
• Collect, enter, and manage study data in REDCap and other databases.
• Perform data quality checks and track enrollment and regulatory deadlines.
• Contribute to mentored research projects such as abstracts, posters, or manuscripts.

Skills

Regulatory coordination

Informed consent

Interpersonal communication

Data collection

Regulatory compliance

Education

Bachelor's degree in STEM or Psychology

Tools

REDCap

Job description

Boston Children’s Hospital’s Cardiovascular, Critical Care and Perioperative, Patient Services team is seeking a Part-Time Clinical Research Assistant (Nursing Research). You will support nurse-led projects, coordinate trials, and work with investigators and clinical teams to ensure studies meet standards and procedures.

Responsibilities include IRB submissions, patient enrollment, REDCap data entry, data quality checks, and contributing to abstracts and posters.