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clinical research in Houston

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  1. 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 ...

  2. Clinical Research Associate

    We are partnering with two top performing CRO companies on a confidential search for  Regional Clinical Research Associates to join their expanding field monitoring team. This role is responsible for the clinical monitoring of designated projects in accordance with applicable SOPs, ICH and GCP guidelines. Responsibilities include performing clinical on-site monitoring activities, collecting regulatory documentation, performing qualification, initiation, monitoring and termination of investigational ...

  3. CRO Seeking Senior Quality Assurance Auditor

    If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further! Precept Life Sciences is partnered with a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Our client has one of the largest global footprints of any CRO today and is committed to not only maintain their standards, but to continue to strengthen their presence even further! They offer a ...

  4. 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 ...