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Senior Clinical Research Associate

Senior Clinical Research Associate

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Senior Clinical Research Associate

  • Location:

    United States of America

  • Sector:

    Clinical Research - Pharma

  • Contact:

    Arslan Sabir

  • Salary:

    Competitive

  • Job type:

    Interim/Contract

  • Contact email:

    pharmajobs@msigroupltd.com

  • Job ref:

    VR/03981_1669051687

  • Published:

    17 days ago

  • Duration:

    12 Months

MSI is looking for Experienced Clinical Research Associates who are looking to grow with a Global CRO based in the USA.

It is a homebased role with regional travel and the CRO is offering roles within exciting therapeutic areas!

Education and Experience:

  • Minimum 3+ year of Independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation
  • Ability to manage required travel of up to 60% on a regular basis
  • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements

What you'll do

  • Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
  • Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
  • Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
  • Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines while also Ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
  • Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
  • Execute. Monitor completeness and quality of Regulatory Documentation and perform site document verification.

If you are interested then email me at