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Hi,We at Verna Scientific delivers custom client-centric solutions by offering contract outsourcing and premium staffing to the most well known life science/telecom organizations throughout United States. Our vision is to become a most reliable 'connector' between pharmaceutical, Biotechnology, Medical Devices and Talent pool i.e ' YOU '.We have following opportunity currently available for you. Job Title: Clinical Research Associate IILocation: Marlborough, MA Description:Employees independently support planning, preparation, execution and closeout of clinical trials. They begin to establish cross-functional relationships. Employees should develop all of the critical competencies before progressing to the next level Track Screening & Enrollment and identify issues. ? Independently confirm that site regulatory documents match Study Master File (SMF). Contact sites on a consistent basis to assess study compliance. Address non compliance issues at investigative site and develop CAPA if necessary. Actively manage EDC remotely. Reviews Project Plan. Write confirmation letter, site visit report and follow up letter. Train new study coordinators on ICH/GCP guidelines and study specific requirements. Identifies adverse events during monitoring and ensures sites complete appropriate reporting. Assists in reviewing medical publications. Assembles portions of clinical protocols in development under guidance of Sr. CRA and Project Manager. Requirement:Bachelors Degree in Science or Healthcare Related Field. Professional Experience Years: 2-4 years experience in clinical/scientific research, medical device/pharmaceutical clinical trial experience. I appreciate if you forward your updated resume, availability (if you are authorized to work in the United States for any employer), location and position preferences at for review before we speak.Also if you have any friends or colleagues, working on similar skill set, kindly forward this mail to them as well, as there are multiple positions.ThanksGlenn