Associate Cra

hace 7 días


Desde casa, México IQVIA A tiempo completo
Whether you're beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You'll have training and development to plan and progress your career in the direction you choose.

And you won't do it alone - you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.


Award winning and innovative, we'll give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries.

You'll be building a smart and flexible career with no limits.

While projects vary, your typical responsibilities might include:

  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

The CRA training duration is 6 months (upon performance
)
You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

You should have:

  • A Bachelor's degree in a health care or other
    scientific discipline or educational equivalent.
  • Advanced in
    English.
  • Availability to
    travel (70% of the time).
  • Based on
    Mexico City (hybrid role).
  • Successful completion of a CRA Trainee Program (highly valued but not mandatory).

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