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ECOG Introduction to ECOG Clinical Trials Guide For Cancer Patients What is a clinical trial? Why participate? Does insurance cover costs? What if I change my mind? How can I join a clinical trial? ECOG's active protocols Educational Materials Selenium E5597 GI Studies E4203,E5204 GI E1208 Head & Neck Cancer E1305 Lung Cancer E1505 Lung Cancer E5508 Lymphoma E2410 Melanoma E1609 Melanoma E2603 Prostate CHAARTED E3805 Cancer in Siblings E1Y97 Non-Hodgkins Lymphoma E4402 Breast E2108 Breast Cancer PACCT1: TAILORx Informational Videos Trial Summary Results Pathology and Laboratory Science Pathology and Lab Science Trial Monitoring ECOG Data Monitoring Committee ECOG Institutions Institutions by state Alphabetical listing Joining ECOG Joining ECOG Publications Publications bibliography Announcements Job Openings Future ECOG Meeting Dates Researcher Advocate Partners Young Investigator Symposium Cobb Institute/NMA Symposium - Colon and Rectal Cancer CME Modules Available Scales and Criteria ECOG Performance Status Common Toxicity Criteria Cancer Information Colon Cancer Video Cancer Survivor Publications Releasing Results Guidelines Other Cancer Sites ECOG Main Institutions' Sites Other Cooperative Groups Advocates/Support Groups PrECOG, LLC 
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Join the fight against cancerThe following positions are open:
Quality Assurance/Quality Control Project Leader for Clinical Trials (Job Code: QAWS)
Position Summary: The QA/QC Project Leader is responsible for the day to day operations of the QA/QC team. They are responsible for ensuring the team is working to achieve their main objectives. These include, primarily, to ensure adherence to standard ECOG data management procedures and to study-specific data management SOPs.Secondary objectives include: To identify and recommend training needs for an individual, study team, or the Data Management Department, To advise the Data Management Department of noted obstacles that hinder the quality, accuracy, or reliability of data. To recommend improvements to the Data Management Department's standards and processes. Essential Job Functions: Oversee the implementation and management of ECOG's Data Management Quality Assurance/Quality Control Program, under the direction of the CDM Manager. Institute policies and procedures to ensure the accuracy and consistency of data management practices Author related SOPS, WI, and other documentation and tools to enhance the functioning of the QC program Assist with the development, implementation and oversight of the Data Management QC database Supervise, train, and mentor Data Management QC auditors Provide case related feedback to data associate, project coordinator and project manager (as appropriate) Assess relevant training needs for staff in consultation with departmental manager, including assessment methods and measurement systems Works with Managers, Project Leaders, and Project Coordinators to assess and identify training needs Perform QC against DB Following up on deviation, incident and audit corrective actions Providing periodic reports to management regarding status of audits and corrective actions Oversee the development and evaluation of the case audit tool throughout the conduct of a study and revise as needed Advise management of any observations about study conduct at clinical sites Ability to maintain confidential information Ability to provide effective feedback in a sensitive and diplomatic manner Ability to maintain an objective and neutral perspective when evaluating the work of fellow coworkers. Qualifications: Bachelor's degree or equivalent work and/or life experience A minimum of three year experience in clinical trials required QA/QC experience and experience using Oracle Clinical Strong computer skills with proficiency with Microsoft Office, Ingres tools, data retrieval, Protrac an advantage Excellent leadership, organizational, and interpersonal skills Excellent written and verbal communication skills Excellent organizational and prioritization skills, work under pressure and meet deadlines Experience or education in medical or scientific area an advantage, particularly oncology Knowledge of Data Management principles for multi-site clinical drug trials required Knowledge of Good Clinical Practices (GCP) Travel to our bi-annual group meeting may be required. Full Time, 40 hour position, Monday -- Friday during normal business hours (8-4 or 9-5).
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