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clinical research in Kansas City

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  1. Senior Clinical Research Associate

    We are looking for CRAs with at least 6 years monitoring experience and 3-4 years in Oncology .  .   Responsibilities: MONITORING – Preparation, conduct, and reporting of selection, initiation/startup, routine/interim and closeout monitoring visits, Site management, Assistance at internal and third-party audits).  Assures timely reporting of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations.  Maintains regular review of site regulatory binder and ensures proper storage, ...

  2. Senior Clinical Research Associate

    We are looking for Midwest CRAs with at least 6 years monitoring experience and 3-4 years in Oncology .  .   Responsibilities: MONITORING – Preparation, conduct, and reporting of selection, initiation/startup, routine/interim and closeout monitoring visits, Site management, Assistance at internal and third-party audits).  Assures timely reporting of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations.  Maintains regular review of site regulatory binder and ensures proper ...

  3. $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 / ...

  4. Home-Based Clinical Research Associate

    Precept Life Sciences is seeking experienced Regional CRAs across the country for permanent positions with several leading CROs. On average, CRAs are assigned to an average of 12 sites across 1-3 protocols. Study and site assignment will vary depending on monitoring duration/frequency, location of sites and complexity of trial. CRAs are expected to be 80% billable, with approx. 60% travel. We are looking for CRAs that are not just field monitors, but those that manage all aspects of the site ...

  5. Sr. SAS Programmer

    Precept Life Sciences is currently seeking several SAS Programmer/Sr SAS Programmer for a permanent position with our pharmaceutical client.  THESE ARE RELOCATION OPPORTUNITIES TO EITHER RALEIGH, NC or ELLICOT CITY, MD. The individual will be part of the Research and Development Group (R&D) which is responsible for all FDA related research and supports all non-FDA company sponsored research. Responsibilities: Primary Job Responsibilities:   Program, update and maintain SAS programs to produce ...

  6. Clinical Project Manager (Global/Oncology)

    Global PM Desired Skills & Experience •          College/University degree in life sciences, RN preferred •          At least 5 years of prior industry experience •          At least 2 years of experience at a position of Clinical Project Manager •          Previous CRO experience required •          Therapeutic experience - Oncology. •          Participation in at least three clinical research projects in the capacity of a Clinical Project Manager •          Proficiency in standard MS Office ...

  7. Senior Clinical Research Associate

    We are looking for a Midwest CRA with Oncology and Infectious disease.  Must have both therapeutic areas to be considered.   Responsibilities: MONITORING – Preparation, conduct, and reporting of selection, initiation/startup, routine/interim and closeout monitoring visits, Site management, Assistance at internal and third-party audits).  Assures timely reporting of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations.  Maintains regular review of site regulatory binder and ...

  8. Senior Clinical Research Associate

    We are looking for a Midwest CRA with Oncology and Infectious disease.  Must have both therapeutic areas to be considered.   Responsibilities: MONITORING – Preparation, conduct, and reporting of selection, initiation/startup, routine/interim and closeout monitoring visits, Site management, Assistance at internal and third-party audits).  Assures timely reporting of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol deviations.  Maintains regular review of site regulatory binder and ...