Research Data Specialist - Breast Oncology Cohort Studies Program
reputed company 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 reputed company 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 reputed company 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 reputed company 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 reputed company investigators, IS staff, and clinic staff in the reputed company development of the CRIS system
- Assist reputed company 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 reputed company data collection, reporting, analysis and audits
- Ensures timely reporting to reputed company reputed company data repositories, including national repositories reputed company 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
- reputed company QA and QC procedures to ensure reputed company data reporting as assigned
- reputed company knowledge of specialized data sources specific to reputed company data reporting, including routine reaching out to offsite providers to obtain information from medical records at reputed company 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 reputed company reputed company 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 reputed company Office
- Experience of 0-1 years in a medical, scientific research, or technology-oriented business environment
Company Overview
Company H1B Sponsorship