Posted in Other about 11 hours ago.
Location: Boston, Massachusetts
Site: The General Hospital Corporation
At Mass General Brigham, we know it takes a surprising range of talented professionals to advance our mission-from doctors, nurses, business people and tech experts, to dedicated researchers and systems analysts. As a not-for-profit organization, Mass General Brigham is committed to supporting patient care, research, teaching, and service to the community. We place great value on being a diverse, equitable and inclusive organization as we aim to reflect the diversity of the patients we serve.
At Mass General Brigham, we believe a diverse set of backgrounds and lived experiences makes us stronger by challenging our assumptions with new perspectives that can drive revolutionary discoveries in medical innovations in research and patient care. Therefore, we invite and welcome applicants from traditionally underrepresented groups in healthcare - people of color, people with disabilities, LGBTQ community, and/or gender expansive, first and second-generation immigrants, veterans, and people from different socioeconomic backgrounds - to apply.
Job Summary
The Cancer Center Protocol Office is seeking motivated, detail-oriented individuals to join our team as a Clinical Research Data Specialist (CRDS). The Cancer Center Protocol Office is a centralized research office that supports clinical researchers in all disciplines within the Cancer Center. Our office promotes and facilitates clinical research by providing comprehensive services to physicians conducting clinical trials while ensuring compliance with all regulatory requirements.
The CRDS works independently under minimal supervision to extract clinical data and research data from electronic medical records and other sources and enter into electronic data capture system utilized for the clinical research protocol. The CRDS will be responsible for entering data for multiple oncology clinical trials. This position is fully remote.
Qualifications
PRINCIPAL DUTIES AND RESPONSIBILITIES:
The CRDS will perform the following responsibilities independently under minimal supervision by the Clinical Research Manager:
• Obtain and abstract complex clinical information from multiple sources (medical records, research records, etc.) for research subjects.
• Record information into various study-specific data-capture systems (both electronic and paper-based).
• Resolve and answer data queries with minimal errors.
• Perform standard data management quality control steps.
• Maintain awareness of details of clinical data to identify missing or inaccurate data; and track data inconsistencies for Clinical Research team to review and report accordingly
• Work professionally with sponsor representatives to review and correct data recorded in the case
report forms.
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