Senior Clinical Research Associate (remote-based)

€50000 - €60000 per annum
  1. Permanent
Madrid, España
  1. Clinical Operations, Project Management
Posted: 23/11/2023

This vacancy has now expired. Please see similar roles below...

Hobson Prior are currently seeking for a Senior Clinical Research Associate to join a fantastic consultancy on a permanent basis with the ability to work remotely. Our client is focused on bringing ophthalmic innovations to market.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

  • For this role, you will handle and uphold information and documentation in CTMS, eTMF and multiple other systems as suitable and per timelines.
  • Responsible for developing solid site relationships and guarantee continuity of site relationships through all phases of the trial.
  • Conducts, with oversight, clinical study site management/monitoring actions in compliance with ICH-GCP, sponsor SOPs, local laws & regulations, protocol, site monitoring plan and affiliated documents.
  • Conduct both remote and on-site supervision and oversight actions using multiple tools to guarantee: data produced at site are complete, precise and unbiased; subject's right, safety and well-being are protected.
  • You will perform site visits which will include to review visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and precise visit & non-visit contact reports appropriately in a timely manner.
  • Recognise, examine and solve site performance, quality or compliance issues and raise as suitable in cooperation with clinical research lead and CRA line manager.
  • Any other assigned duties.


  • Capable of comprehending how to suitably examine an investigative site's abilities to performing clinical research.
  • Able to verify source data to reported data.
  • Demonstrable experience in a CRA or corresponding mix of education, experience and training.
  • Familiarity with ophthalmology would be ideal.
  • Able to regularly examine protocol and GCP compliance.
  • Capacity to supervise and report on the progress of the trial from start-up to accomplishment.
  • Expertise on how to select and qualify an investigative site.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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