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The Clinical Trial Data Analyst is responsible for building programs to create datasets, listings, tables and figures from clinical databases, external data sources, and other sources. In addition, the position coordinates in-house data management activities (including vendor management) to ensure the accuracy and consistency of clinical databases for subsequent analysis and reporting. Responsibilities: Prepare data reports, tables and graphs for regulatory submissions, IRB submissions,....


This position is responsible for leading internal and outsourced Clinical Data Management activities in support of Clinical Research studies, managing the definition of Case Report Form (CRF) requirements, creation of the Data Management Plan, coordination of Centralized Data Review activities (a key component of Risk-Based Monitoring), and is accountable for data integrity, quality, and consistency at Database Lock. The employee must be able to lead data review activities and engage different


We have immediate openings for senior-level civil engineers with strong technical abilities and experience in transportation project design and the ability to lead a team of engineers on small and large projects. Can work in any of these offices**** - Pleasanton, Sacramento, Oakland, Newport Beach - They need 1 in each office! Accelerate your civil engineering career and promote yourself. Work on marquee projects, with a collaborative team in a vibrant environment, and move into Project....

- Irvine, CA

The candidate is responsible for expeditiously developing and processing raw material and product documentation to meet quality requirements within timelines established for product launch and/or timely project completion.The Master Specifications and Documentation department interacts with various Pharmaceutical groups within the organization and departments such as Quality, Global Pharmaceutical Technology, Regulatory Affairs, Operations, Manufacturing (all sites), Procurement (Sourcing),....

- Akron, OH

An opportunity to join one of the award winning children's hospitals in the region. Full time afternoon shift Supervisor to work either five 8 hour shifts (3:30pm to 12 midnight) or four 10 hour shifts (2pm to 12:30pm). Routinely No weekend and holidays! The ideal candidate will be responsible for the following:Plans, coordinates and directs the daily activities of the personnel in assigned sections. Provides expert technical assistance. Directs training of the section personnel. Assigns,....


Plant Quality Manager -- Dairy Product Manufacturing -- SQF -- Excellent Salary, Benefits and relocation assistance This opportunity is with one of our finest client companies. We have placed many people with this firm over the years who have found an unexcelled career opportunity here. Continuous expansion, another new plant opened recently, very much in demand traditional food products! GENERAL DESCRIPTION of the Quality Manager position: The Plant Quality Manager oversees all Quality....


The Associate will be responsible for supporting CTM/OSL and ensuring that all assigned clinical study(ies) are running on time and on budget and are completed in compliance with all relevant laws, regulations, and regulatory guidelines as well as all policies and procedures. Requirements: Bachelor’s degree or higher (science degree preferably in science or health-related field) Previous experience of working on a clinical study 1-2 year relevant experience in pharmaceutical industry or CRO....


We are in search of a Medical Director for a corporate site focused on worksite-based health and wellness center serving company employees. This is a NEW role located near Wichita, KS… rated as one of the best places to live in 2018 and known for having some of the best public schools in the country. There are 8400 employees eligible for care at this site. Matching 401k, 34 paid days off, CME allowance, and more. Relocation and possible sign on bonus. Salary starts at $ 200K and goes up quite....


Summary We are currently accepting resumes for the position of Research Scientist in Analytical R and D/Methods Development and Validation. ResponsibilitiesMust be fully capable of developing analytical methods based on experience, literature search, etc.Design, develop, conduct and/or review experiments including method development and methodtransfer; perform methods validations utilizing typical instrumentation including but not limited to LC,MS, GC, etc.Interpret data from routine and....


POSITION SUMMARY The Analytical Instrumentation Manager will be responsible for the management of daily activities in support of all analytical equipment in Quality Control. The manager will assure that activities associated with the testing, release and results reporting of materials, products and components meet established and expected quality, Data Integrity requirements, regulatory and customer requirements. The Manager will regularly interact with departments on site and at a corporate....


Our client is a well-established, growing Clinical Research Organization (CRO) seeking a Senior Clinical Trial Manager/Project Leader located in our Frederick or Rockville, Maryland office. Our client has been named a top workplace by the Washington Post and offers exceptional career opportunities.Their studies impact public health initiatives on a global scale occurring in more than sixty countries spanning across six continents. They are dedicated to providing statistical and epidemiological

- Wichita Falls, TX

If you are seeking to join a growing company which offers personal growth opportunities, this position as HVAC Mechanical Engineer may be the one for you. Our client is a leading manufacturer of quality commercial HVAC equipment since 1955. The company has a history of strong sales growth, driven by superior service and new product development. Continued growth projections have created a growing opportunity for experienced manufacturing professionals. Independently owned and operated, the....


Senior Program Manager - Clinical Development and Clinical Studies (long-term contract 2 year minimum) Our client, a privately-owned Contract Research Organization (CRO) employing over six hundred staff worldwide with offices located in Rockville, MD, Frederick, Maryland, Vancouver, Canada and Bangalore, India, has a new opening supporting a new exciting initiative to cure Sickle Cell Disease. Project Management - Program Management - Genetic Therapeutic Science The National Heart, Lung, and....

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