Posted
Mon., Sept. 13
Organization
The Mucosal Immunology and Biology Research Center
Position Description
The Mucosal Immunology and Biology Research Center at Massachusetts General Hospital is seeking a Clinical Research Coordinator I for a Phase 2a (Proof of Concept) clinical trial study.
Responsibilities include:
- Screening and determining subject eligibility required for participation
- Conducting/assisting with baseline assessments to determine entry eligibility
- Speaking with patients to execute recruitment for clinical trials,
- Providing explanations of study trial to patients and families,
- Interviewing study participants to collect accurate study data
- Administering and scoring questionnaires
- Assisting with collecting, processing, and shipping a variety of study related samples
- Obtaining informed consent from subjects for studies, in accordance with hospital policy
- Facilitating and conduct follow-up visits with participants following study timeline
- Facilitating clinical laboratory testing and other study related assessments
- Preparing regulatory documents
- Developing and managing study survey to meet goals
- Assisting in budget reviews
- Composing and amending consent forms, protocol summaries, and other documents for sponsor and/or IRB review
- Managing study related Insight e-IRB applications
- Ensuring that study documents are stored, maintained, and routed in compliance with applicable federal, hospital, departmental, and study-specific regulations.
- Maintaining study records including logs
- Working to resolve data queries and ensure that data in electronic databases are accurate
- Assisting with the development and maintenance of RedCap database
- Reviewing patient medical records to assist with identifying study candidates
- Assisting with preparing safety reports and other study progress reports for PIs to review
- Ensuring that PI groups receives results of study tests and procedures
Position Requirements
- Bachelor's degree
- Computer literacy, including Office Outlook, Excel, and Word.
- Working knowledge of clinical research protocols
Time Commitment
Full-time
Compensation
TBD
Apply
To apply, please both email your CV/resume to Rosie Lima and apply here.
