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clinical research in Dallas

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  1. (Senior/Lead) SAS Programmer -Remote USA

    Great opportunity for Senior to Lead SAS Programmers. Competitive, salary, benefits package, and bonus available.   Responsibilities include: •Acts as the lead programmer on multiple studies •Manages project timelines, budgets, and resources •Effectively assigns and communicates priorities and work direction to ensure completion of assigned tasks on time and within budget •Oversees the programming aspects of clinical trials from data extraction from trial databases through analysis and reporting, ...

  2. (Senior/Lead) SAS Programmer -Remote USA

    Great opportunity for Senior to Lead SAS Programmers. Competitive, salary, benefits package, and bonus available.   Responsibilities include: •Acts as the lead programmer on multiple studies •Manages project timelines, budgets, and resources •Effectively assigns and communicates priorities and work direction to ensure completion of assigned tasks on time and within budget •Oversees the programming aspects of clinical trials from data extraction from trial databases through analysis and reporting, ...

  3. CRA - Minimal Travel and Sign On Bonus!

    ***$5,000 Sign On Bonus***   Locations: Dallas, TX Evansville, IN Madison, WI   We have facilities in these cities where CRAs will work daily with minimal travel.   MUST have Phase I experience!   Now is the time to join our growing business where you have supportive management and a cohesive team.   At Covance, you are not just a number. We value you and your hard work...we want you to succeed – better yet, we want you to GROW your CAREER!   COVANCE is focusing on balance and quality ...

  4. Senior Clinical Research Associate

    Senior Regional Clinical Research Associate Identifies potential investigators, contract research organizations and outside vendors. Collects required documentation for review by Project Manager to make a selection decision. Conducts site visits pre-study, at study initiation, at regular intervals during the study and at study closeout. Prepares a variety of reports and letters in accordance with study SOPs and industry standards. Collects, reviews and processes regulatory documents. Ensures ...

  5. Clinical Operations Lead

    Please note we have 3 different openings in the below locations: 1 position available in Southern Calfornia 1 position available anywhere in Florida 1 position available anywhere in Texas Contract Length:  12 months Pay Rate: to be discussed via phone - great rate  Target Start Date: August Starts REQUIRED: Training and Education:          A scientific or technical degree in the healthcare area is preferred along with extensive knowledge of clinical trial methodology.          In general, ...

  6. Clinical Trials Assistant-3972226

    Job Purpose -  Assist Clinical Trial Management to ensure accurate, timely, and coordinated availability of clinical trial materials and documents.  Mentor and assist with training of incoming CTAs.  Assist with process improvement efforts.   Skills- Major Accountabilities - 1.  Enter and maintain current data in clinical systems (i.e., enrollment as requested, EDC access maintenance, etc.) 2.  Coordinate printing of Investigator Study File (ISF) and other study materials and distribution to ...