Research Data Specialist - Breast Oncology Cohort Studies Program
Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. They are seeking a Research Data Specialist to support the Breast Oncology Cohort Studies program by managing clinical data collection and biospecimen organization related to patients with germline mutations.
Responsibilities
- Responsible for reviewing and abstracting the medical records for research patients on trials they are assigned
- Entering identified clinical data points in the corresponding database
- Ensuring that data is entered within the outlined timelines for each trial
- Assisting research teams with the development, testing and implementation of Case Reports Forms for PI-Initiated clinical trials
- Evaluating and tracking the eligibility of all patients seen in the clinic for inclusion in the study
- May assist or be responsible for consenting eligible patients in clinic
- Maintaining on-going communications with Information Services and physicians and staff for data collection needs
- Reviewing and abstracting the medical records for patients. Entering the clinical data into the Clinical Research Information Systems (CRIS)
- Accessing patient demographic and clinical information from the clinical systems. Entering information into the database
- Reviewing data for quality and completeness using reporting software
- Collaborating with principal investigators, IS staff, and clinic staff in the continued development of the CRIS system
- Assist principal investigators and staff in the creation of data reports for quality assurance measures
- Coordinates the collection, processing, organization, and storage of biological specimens including maintenance of electronic specimen tracking systems (STIP) and laboratory binders
- May be responsible for IRB and regulatory submissions and maintenance of regulatory files
- Support the clinical programs with outcomes data collection, reporting, analysis and audits
- Ensures timely reporting to internal and external outcomes data repositories, including national repositories when required by regulatory requirements and U.S. law
- Ensure case management documentation in patient medical records and other information management systems as assigned to support clinical program clinical care
- Perform QA and QC procedures to ensure optimal data reporting as assigned
- Develop knowledge of specialized data sources specific to outcomes data reporting, including routine reaching out to offsite providers to obtain information from medical records at outside sites of care
Skills
- Bachelor's degree or 1 year of experience as a Dana-Farber Associate Research Data Specialist
- Excellent organizational and communication skills required
- Strong interpersonal skills – ability to effectively interact with all levels of staff and external contacts
- Must be detail oriented
- Ability to effectively manage time and prioritize workload
- Must practice discretion and always adhere to institutional confidentiality guidelines
- Must have computer skills including the use of Microsoft Office
- Experience of 0-1 years in a medical, scientific research, or technology-oriented business environment
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