This person will participate in the day-to-day management of CRO Data Management activities (i.e., development Data Management Plan (DMP), develop and annotate CRF's, develop database specifications, design or oversee the development of edit check specifications and programs, adherence to timelines and data expectations, etc.
Leading Pharmaceutical fortune 200 company with over 25,000 employees globally is seeking to expand its team in the Bay Area. While the company is international, this team has more of a small company feel, looking for the right cultural fit for this Sr.
Sales Executive (Used Cars) Ford Morpeth £12,000 basic salary, £35,000 OTE with uncapped bonus, company benefits and Company Car Overview You will see from our website and our recent financial results that we are a rapidly becoming one of the Country's leading automotive retailers.
POSITION SUMMARY: To provide SAS programming support for the Clinical Research Programming Department. ESSENTIAL FUNCTIONS:1. Develop and document programs to create analysis datasets summarizing key clinical trial data. 2. Develop and document programs and to produce tables, listings and other reports and analyses summarizing clinical trial results.
Client located in the East Bay has an immediate need for a Principal SAS Programmer. The Principal SAS Programmer provides technical leadership in SAS and other programming support with respect to design, conduct and analysis of clinical trials.
I am currently urgently recruiting for a mechanical design engineer for a medical device client of mine located in Dublin, CA. This is a large, reputable medical device client that is looking for an experienced, hands-on design engineer to work within their team.
A board certified oncologist/hematologist with industry experience who will report to the Chief Medical Officer and work collaboratively with the Clinical Study Team contributing to the strategic planning and execution of Clinical Development Plans for all compounds in clinical development.
Initiate and lead clinical study teams as clinical director. Responsible for the successful operations of all study teams to achieve the study objectives at the highest standards and on time and budget.
Rate: $50/hr.Location: Dublin CaProposed Duration: 6 monthsKey note: Person has to have used WPF or Winforms in a professional environment.Sr. Software Engineer is responsible for the development of medical device software, including project planning, requirements analysis, design, implementation, and testing of software.
Headquartered in Atlanta, Georgia-Pacific is one of the world's leading manufacturers and marketers of building products, tissue, packaging, paper, cellulose and related chemicals. The company employs more than 40,000 people at approximately 300 locations in North America, South America and Europe.
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