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You will be updated with latest job alerts via emailQUALIFICATIONS:
In order to be eligible for an interview the following skills are necessary: previous clinical work including consenting patients.
Bachelors degree required.
1 year of experience in a similar research setting.
SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:
Experience using Microsoft Excel Access and Word are required.
Experience using Electronic Medical Records for data collection and review is preferred.
Knowledge of clinical research protocols and clinical trials process with at least 2 years clinical research experience is preferred.
Knowledge of medical terminology.
Ability to demonstrate professionalism and respect for subjects rights and individual needs.
Excellent interpersonal skills are required for working with the study participants.
Careful attention to detail.
Good oral and written communication skills.
WORKING CONDITIONS:
Data office operating room and laboratory working conditions include working under pressure to meet deadlines and meetings moderate stress thus the workload could necessitate occasional evenings.
DRESS CODE:
Professional dress code required. No jeans sneakers shorts or teeshirts
GENERAL SUMMARY/ OVERVIEW STATEMENT:
The Clinical Research Associate II is responsible for all administrative and operational aspects of clinical research within the Thoracic Surgery Division. He/she monitors patient accrual to surgical trials at the Brigham and Womens Hospital (BWH) and DanaFarber Cancer Institute (DFCI) including actively recruiting patients on trial following patients through the protocol treatment program and followup and completing data forms and data management required by the studies. Facilitate and coordinate IRB reviews and submissions.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
1.Responsible for collecting data and maintaining patient information database for studies.
2.Responsible for and proactively manages IRB and other regulatory submissions for protocol submissions and updates renewals adverse event reports deviations data audits etc.
3.Complete data analysis and run various reports.
4.Interacts with patients/subjects with regard to consenting data collection followup and other tasks as assigned. May serves as a liaison between patient and physician.
5.Performs quality control procedures to ensure integrity of data in clinical research database as determined by PI and Manager.
6.As required collects biologic samples and specimens and ensures protocol adherence in the operating room laboratory and intensive care settings per study guidelines.
7.Answers any phone calls and inquiries regarding clinical research database or study protocol. Refers participants when appropriate to supervisor or clinical staff.
8.Participates and assists in training and orienting new research assistants and staff.
9.All other duties as assigned
Shift:
Day
Brigham and Womens Hospital is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race sex color religion national origin sexual orientation protected veteran status or on the basis of disability.
Full-Time