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Job Overview As a market leader in central laboratory, pre clinical services and clinical trial management services, Covance works with most leading pharmaceutical and biotechnology companies to life saving medicines to patients in need sooner. Over the past 10 years we have handled over 10,000 clinical trials in more than 600 indications, worked with over 200 thousand investigators, and collected
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Job Overview Reporting to the Vice President, the primary role of the incumbent will be to provide subject matter and drug development expertise in support of clinical drug development trials in rare diseases as well as pediatric patient populations. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Executive Medical Direct
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Design and develop materials using sound instructional design practices such as the ADDIE model and applying Adult Learning Principles Utilize multiple delivery and distribution channels including e learning, web based, instructor led, virtual classroom, mobile, and social collaborative learning programs Use instructional design and multi media tools (Articulate Storyline, Adobe eLearning Suite an
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Job Overview The primary focus of the Associate Director, Client Engagement is to provide Quality Assurance support for decentralized clinical trial activities. This will include facilitation of quality issue investigation and CAPA development as well as identifying trends/signals from non compliance data, and partnering with the business and sponsors to develop risk mitigation strategies. This in
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Job Overview The Senior Manager QA Process Lead position is an individual contributor that has responsibility for oversight and delivery of the Internal Process Compliance function activities. This position and department will be aligned as partners to the functional areas of the Clinical Development and Commercialization Services (CDCS) business to ensure appropriate quality/compliance oversight
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Individual diagnostic evaluation and case sign out of primarily Gynecologic pathology specimens. Assure compliance with quality, regulatory, and safety guidelines/standards A ccurate and timely evaluation of specimens tested Assures good laboratory practice (GLP) and compliance with applicable accrediting and regulatory agencies Provide expert consultation as needed with clients and staff, in pers
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include, but are not limited to the following Develop omni channel campaign strategy Collaborate with Product Marketers and other stakeholders to understand business goals, market sizing and insights, and product positioning Perform consumer research (competitive, comparative, and keyword) to influence campaign strategies and budget Create journey maps for key audiences to impact key messages and
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Job Overview Whether it's at home, school, the office or other alternate location, Covance provides mobile clinical services for clinical trial patients to make it easier for patients to participate in a clinical research study. Our Mobile Clinical Services team is seeking a Learning and Content Delivery Manager. This position can be homebased anywhere in the US. Some travel, both domestic and int
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Job Overview Hiring forSeniorStatistical Programmer (Remote) FSP can be based anywhere in USA/ Canada#LI REMOTE Develop SAS programs for SDTM, ADaM, client defined analysis datasets, Patient Profiles, Tables, Listings and Graphs in support of the Statistical Analysis Plan, posters, manuscripts, Integrated of Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) Provide technical plannin
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Job Overview Individual has responsibility for coordinating the activities of routine and non routine studies for in vivo PK in compliance with appropriate company standards, GLP, GCP, GMP and regulatory guidelines specified in the study plans, protocols, or work agreements governing the work in which they areinvolved in a timely, efficient and quality manner. Trains and mentors less experienced s
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Job Overview Covance by Labcorp is the word'd largest CRO, offering a variety of career opportunities and growth potential in the world of drug discovery. Jumpstart your career and make a positive impact in biopharmaceuticals by joining our large molecule, BioAnalysis laboratory in Somerset, NJ. We are seeking a Research Assistant II with at least 3 4 years of Immunoasssay experience with ELISA, l
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Design and coding of new applications and enhancing existing applications. Pushes the envelope with innovative and creative thinking Provide leadership to projects to help deliver quality product Architect solutions and determine optimal utilization of services on AWS Contributes to the micro services standards for the company Performs code and design reviews with peers. Education/Qualifications M
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Job Overview The Contracts Specialist I, Site Agreements will be remotely (home based) located anywhere within the United States. 1. Responsible for adherence to standard operating procedures (SOPs). 2. Perform the following, with occasional guidance from line management or more experienced colleagues daily tracking, negotiation and approval of Site Agreements and Site Agreement templates (as appl
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Job Overview Hiring forSeniorStatistical Programmer (Remote) FSP can be based anywhere in USA/ Canada#LI REMOTE Develop SAS programs for SDTM, ADaM, client defined analysis datasets, Patient Profiles, Tables, Listings and Graphs in support of the Statistical Analysis Plan, posters, manuscripts, Integrated of Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) Provide technical plannin
Posted Today
Job Overview Hiring forSeniorStatistical Programmer (Remote) FSP can be based anywhere in USA/ Canada#LI REMOTE Develop SAS programs for SDTM, ADaM, client defined analysis datasets, Patient Profiles, Tables, Listings and Graphs in support of the Statistical Analysis Plan, posters, manuscripts, Integrated of Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) Provide technical plannin
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