Cardiology Research Assistant II: Study Coordination & Data

Boston Medical Center; Boston (MA); On-site; USD 25,000 - 35,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

Pharmacy benefits

Flexible Spending Accounts

403(b) savings matches

Paid time off

Career advancement opportunities

Well-being resources

Job summary

Boston Medical Center is seeking a Research Assistant II to coordinate subject recruitment, enrollment, follow-up, and data collection for cardio research projects. The role involves screening participants, obtaining informed consent, and ensuring study conduct meets regulatory standards.

You will enter data, transcribe questionnaires, code qualitative data, and participate in study meetings. Strong English communication, attention to confidentiality, and proficiency with MS Office are

Qualifications

• Bachelor's degree in related discipline is required.
• Masters degree a plus; With a Master's Degree, no work experience is required.
• Knowledge of medical terminology is required.

Responsibilities

• Coordinate and implement subject recruitment, enrollment, follow-up, data collection and study conduct.
• Identify and screen research subjects, recruit and maintain follow-up, obtain informed consent.
• Perform data entry, transcription of questionnaires and coding of qualitative data.
• Participate in study meetings and perform other administrative tasks supporting clinical studies.

Skills

Excellent English communication

Bilingual or multilingual

Cultural sensitivity

Organizational skills

Microsoft Office

Data management

Statistical analysis tools

Education

Bachelor's degree in related discipline

Master's degree preferred

With a Master's Degree, no work experience required

Tools

Microsoft Access

SPSS

SAS

Minitab

Excel

Job description

Boston Medical Center is seeking a Research Assistant II to coordinate subject recruitment, enrollment, follow-up, and data collection for cardio research projects. The role involves screening participants, obtaining informed consent, and ensuring study conduct meets regulatory standards.

You will enter data, transcribe questionnaires, code qualitative data, and participate in study meetings. Strong English communication, attention to confidentiality, and proficiency with MS Office are