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The Separation Sciences group in Discovery Chemistry at our client in Boston, MA is seeking a candidate to join their team whose mission is to analyze and purify novel medicines prepared by their medicinal chemist colleagues.
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As an integral member of the pharmacy team, the Clinical Trials Pharmacist is responsible for coordinating, collaborating, and providing expertise in support of drug clinical trials. Dispenses research medication to subjects enrolled in clinical trials.
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Reviews clinical trial and non-human primate data ensuring integrity, privacy, consistency and compliance for multiple trials at a time. The Clinical Trials Monitor (CTM) monitors and audits the investigator-initiated clinical research studies across all disease groups in the Cancer Clinical Trials Office.
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Primary user of Lawson LBI, SDK, and the Boston Medical Center CTO Clinical Trials Management System (CTMS) Ensures clinical trial accounts and SDK accounts are set up appropriately and supports the study team in the financial management of clinical trials.
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Uses management skills to ensure disease groups have appropriate internal organization to effectively comply with regulatory requirements for clinical trials. Day (United States of America)The Clinical Trials Specialist II is responsible for fostering and enhancing inter-team and inter-group collaboration, serving as a source of knowledge and expertise that can be used as a resource by more junior staff.
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Plans, conducts, and reports on preclinical and clinical studies, including studies for product registration and post-marketing (primarily, but not limited to studies in United States).
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Parexel is an equal opportunity employer. Initiating pre-purification and post-purification analysis of submitted samples by LCMS (liquid chromatography - mass spectrometry). The Separation Sciences group in Discovery Chemistry at our client in Boston, MA is seeking a candidate to join their team whose mission is to analyze and purify novel medicines prepared by their medicinal chemist colleagues.
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Reporting to the Senior Director, Clinical Trials Office, the Associate Director, Clinical Trials Operations is responsible for the overall management and oversight of the assigned Clinical Research Disease group managers.
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The Research Informatics Operations (RIO) Director, Account Services for Clinical Trials Research will work closely with Dana-Farber clinical research stakeholders and functional leaders within I&A to identify, prioritize, and address the clinical research data informatics needs of DFCI.
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Provides guidance to GPS ICSR processing staff on technical aspects of clinical trials and managed access programs, including configuration of the Global Safety Database and relevant reporting rules.
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Job Description - Clinical Trials Pharmacist (3279967) Clinical Trials Pharmacist. Acts as a liaison for principal investigators, the research office, sponsors, pharmacy, and the Institutional Review Board (IRB.
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Owns the Trial Master File for assigned trials; ensures appropriate quality oversight and QC of required elements of TMF. The ideal candidate has a track record of executing complex, on-time clinical trials at a biotech/pharma company.
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Oversees and manages domestic, regional and/or international clinical trials conducted at Labcorp Clinical research sites, external sites, and data services projects. Projects generally include full service including multiple moderately complex trials managing multiple vendors and external sites for trials of moderate to high financial value, and may consist of serving in a program oversight role.
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Associate Director Clinical Trials. Knowledge and experience working with legislation and international guidelines (ICH-GCP/CFR) for the performance of clinical research projects. Skilled in using Microsoft Office programs (Word, Excel, Power Point, MS Project) as well as good working knowledge of electronic data systems and technical solutions such as eTMF, IWRS, EDC, etc.
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Reviews from current employees
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Title: trials Company: Parexel in Newton, MA
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