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clinical research in Phoenix

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  1. $5K Sign On Bonus- CRA  Monitors Needed - Set Yourself Up for Success

    CRAs - Join Covance and receive a $5000 Sign On Bonus! Meet the CRA hiring team at the ACRP conference - email [email removed].   Set yourself up for SUCCESS with Early Clinical Development! 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.   URGENT Need for Oncology Monitors! Calling all Experienced Clinical Research Associates / CRAs / Monitors ...

  2. 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 ...

  3. Senior Clinical Research Associate

    A dynamic and growing CRO is looking for a regional CRA. Responsibilities include but are not limited to: performing monitoring visits including site qualification, initiation, monitoring and close-out visits; maintaining regular contact with study site to ensure protocol/GCP compliance; participating in Investigator meetings and other study training meetings as required; preparing for and participating in Sponsor and FDA audits. Required qualifications: Proven success in monitoring clinical ...

  4. Regional Clinical Research Associate

    Regional Clinical Research Associate The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of ...

  5. Director of QA

    Qualifications * Demonstrated management/supervisor related experience. * Excellent leadership and management abilities. * Strong aptitude in the art and science of quality, CMC, and preclinical procedures and methods. * Good working knowledge and understanding of ICH Guidelines for Good Clinical Practice and Title 21 of the Code of Federal Regulations. * Strong understanding of international regulations regarding clinical research (EMEA, PMDA, Health Canada, etc.) * Experience working closely with ...

  6. Bioinformatics Scientist

      Bioinformatics Scientist Phoenix, AZ Relocation assistance available     Position Summary:                Bioinformatics scientists provide bioinformatics and statistical analysis support for biomarker discovery, IVD product development and CMI tumor molecular profiling service.   Job Responsibilities: ·         Develop and maintain statistical analytical tools and bioinformatics pipelines. ·         Conduct analysis and develop innovative algorithms on biomarker discovery and clinical ...