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Covance
- Princeton, NJ / Nashville, TN / Raleigh, NC
Developing understanding of ICH/GCP, core Clinical Research documentation, soft skills/business communication, clinical trial management, and business client interactions General On Site Monitoring Responsibilities Observe Senior CRAs, CRA 2 and CRA 1 with on site tasks as required and according to training goals (e.g. review of Case Report Forms and Study File Notebook, drug accountability) Engag
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Covance
- Indianapolis, IN / Research Triangle Park, NC
Establish a repeatable, easily manageable process to load industry data sets into global intelligence systems Attend training sessions to learn universal tools linked to MySQL database development Familiarize yourself with business development platforms to analyze and visualize data into valuable insights for more informed decision making Engage in professional development workshops to enhance you
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Covance
- Greenfield, IN / Research Triangle Park, NC
Quickly and efficiently respond to incoming calls and faxes, identify how best to assist. Document calls in appropriate tracking systems, and handle/escalate calls per established procedures. Conduct insurance verifications to understand if patient's prescribed therapy is eligible for coverage. Possibly coordinate prior authorizations, investigate alternative insurance coverage, or other funding s
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What to Expect Data Management, Mining, and Curation Learn about safety assessment data management activities, including considerations for source data and mining and reporting data Prepare data compilations that are used for comparison purposes by scientists when evaluating study data Work closely with data management colleagues, IT, and scientist to identify and develop appropriate data visualiz
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What to Expect Perform basic veterinary laboratory procedures including but not limited to the following duties and responsibilities in compliance with appropriate SOP, Protocol and Regulatory Agency guidelines. Reports all animal care concerns and becomes involved in resolution and appropriate corrective action, when necessary Ensures that studies are conducted according to protocol, standard ope
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Job Overview Co mpany Overview If you've ever taken a medicine, received a vaccine or had blood drawn for a lab test, you've already benefited from the powerful work of 57,000+ exceptional employees across Covance and LabCorp. By supporting leading pharmaceuticals and 600+ biotech companies through our contract research organization (CRO), Covance employees help improve health, improve lives and b
Posted Today
Job Overview Company Overview If you've ever taken a medicine, received a vaccine or had blood drawn for a lab test, you've already benefited from the powerful work of 57,000+ exceptional employees across Covance and LabCorp. By supporting leading pharmaceuticals and 600+ biotech companies through our contract research organization (CRO), Covance employees help improve health, improve lives and br
Posted Today
Job Overview Company Overview If you've ever taken a medicine, received a vaccine or had blood drawn for a lab test, you've already benefited from the powerful work of 57,000+ exceptional employees across Covance and LabCorp. By supporting leading pharmaceuticals and 600+ biotech companies through our contract research organization (CRO), Covance employees help improve health, improve lives and br
Posted Today
Gain an overview of Data Management processes within a clinical trial Perform all data management tasks as appropriate to include, but not to be limited to Design and testing of the Electronic Data Capture (EDC) clinical database Perform ongoing data review including query generation Create and / or update all relevant data management documentation Create study metrics and reports as requested by
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Covance
- Indianapolis, IN / Raleigh, NC
Support the leadership team in building and defining a client playbook as it relates to GSS services and products within the Client Engagement group related to data management and project management functions Understand current process and strategy and help to build a revised process and plan Qualifications Working towards bachelor's degree in business or scientific area Education/Qualifications W
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Intern, Regulatory Compliance Mgmt. Support will assist Data & Technology team members (Regulatory Compliance Mgmt.) in performing various tasks related to completion of Periodic Reviews for regulated/validated data collection systems and execution of Remediation Plans, associated with the Data Integrity program across ED/CTTS. This intern role will be critical in helping to review existing/previo
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Improve efficiency and workflow in the department by completing a process improvement project. Engage in professional development workshops to enhance your business acumen and professional presence Become familiar with the requirements of the FDA Good Laboratory Practices (GLP) Regulations 21CFR Part 58 Learn to perform audits to verify conformance to applicable Standard Operating Procedures (SOPs
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Support the leadership team in building and defining a more robust ICF codification process within the Clinical/Regulatory Operations group Understand current process and strategy and help to build a revised process and plan Building of client training material for ICF codification as our processes have been adjusted Development of ICF codification user interface process review and client visualiz
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Enhance and further develop key business and financial metrics used to inform and guide the business Collaborate with team and business leaders to begin budgetary planning process for the upcoming fiscal year Familiarize yourself with business development platforms to analyze and visualize data into valuable insights for more informed decision making Provides the opportunity to present key finding
Posted Today
Intern, Regulatory Compliance Mgmt. Support will assist Data & Technology team members (Regulatory Compliance Mgmt.) in performing various tasks related to completion of Periodic Reviews for regulated/validated data collection systems and execution of Remediation Plans, associated with the Data Integrity program across ED/CTTS. This intern role will be critical in helping to review existing/previo
Posted Today
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