Job Description
Position Summary
Dr. Rima Rachid, Associate Professor of Pediatrics at Harvard Medical School and Director of the Food Allergy Program at Boston Children’s Hospital is seeking a new Clinical Research Study Assistant (RSA) for her investigative work in the Division of Allergy & Immunology. The CRA will coordinate multiple food allergy research studies, including but not limited to randomized controlled interventional trials on biologics and fecal microbiota transplantation in food allergy, a food allergy biorepository and studies on novel biomarkers in food allergy.
This role potentially involves processing patient's blood and stool samples in the research laboratory.
Key Responsibilities
Education:
Dr. Rima Rachid, Associate Professor of Pediatrics at Harvard Medical School and Director of the Food Allergy Program at Boston Children’s Hospital is seeking a new Clinical Research Study Assistant (RSA) for her investigative work in the Division of Allergy & Immunology. The CRA will coordinate multiple food allergy research studies, including but not limited to randomized controlled interventional trials on biologics and fecal microbiota transplantation in food allergy, a food allergy biorepository and studies on novel biomarkers in food allergy.
This role potentially involves processing patient's blood and stool samples in the research laboratory.
Key Responsibilities
- Consents and enrolls patients for research studies by providing detailed information on the Research Study to patients and families.
- Is responsible for and adhering to all policies and procedures and responds to all inquiries. Obtains informed consent and enrolls patients in research studies.
- Reviews clinical information to identify patients meeting study inclusion criteria. Serves as liaison to the families/patients in the research studies, conducted at both on site and off-site locations, guiding and advising them throughout each phase of the study.
- Coordinates follow up visits as necessary. Acts as a resource to study participants, addressing any concerns they may have. Troubleshoots resolution of any issues that may arise throughout the study.
- Coordinates and prepares documentation needed for Institutional Review Board (IRB) on submissions, for PI approval. Tracks progress from submission to approval.
- Assist in developing supportive study documents such as informed consent forms, monitoring templates, study subject tracking tools, monitoring forms, study manuals, and training materials, as required for a study.
- Assist with the tracking and compilation of enrollment information. May assist with preparation of manuscripts and reports to be submitted to academic journals.
- May help train and orient newly hired study personnel. Coordinates activities with various departments to ensure correct testing/processing and sends clear instructions to each study.
- Monitors and reviews data collection and data entry, and informed consent procedures ensuring consistency of application for each study.
Education:
- A bachelor's degree in a STEM field
- 0-1 years of relevant research experience. No direct post-degree industry experience is acceptable.
Numbers & Facts
| Location | Boston, MA |
Skills
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