Base: $20.16 - $29.01phly; bonus/equity: not speci...
Fully remote
Clinical research protocols knowledge
Patient recruitment for clinical trials
Qualitative and quantitative data collection
Mass General Brigham is seeking a full-time Clinical Research Coordinator (CRC) for the Brain Bioethics Lab in the Department of Neurosurgery. The role involves supporting an NIH-funded study on the ethical challenges of genetic tests for substance use disorders, requiring strong organizational skills and some prior research experience
Job Summary
The Brain Bioethics Lab in the Department of Neurosurgery is seeking a full-time Clinical Research Coordinator to assist with an NIH-funded study on genetic tests for substance use disorders.
This role involves recruiting patients, collecting and analyzing data, maintaining regulatory compliance, and assisting with manuscript preparation.
Mass General Brigham offers competitive base pay, comprehensive benefits, career advancement opportunities, and a supportive team environment.
Matching Summary
Match Score: 85
Mass General Brigham is seeking a full-time Clinical Research Coordinator (CRC) for the Brain Bioethics Lab in the Department of Neurosurgery. The role involves supporting an NIH-funded study on the ethical challenges of genetic tests for substance use disorders, requiring strong organizational skills and some prior research experience.
Salary
Base: $20.16 - $29.01/Hourly; Bonus/Equity: Not specified; Benefits: Comprehensive benefits and career advancement opportunities
Skills & Requirements
Must-have
clinical research protocols knowledge
patient recruitment for clinical trials
qualitative and quantitative data collection
regulatory submissions assistance
data analysis using REDCap and R
Nice-to-have
strong organizational skills
excellent communication skills
ability to work independently and collaboratively
experience with mixed-methods studies
Key Requirements
Bachelor’s degree in related field required
0-2 years post-baccalaureate research experience
experience with IRB and regulatory documentation
experience recruiting participants in clinical settings