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Senior Clinical Research Associate - Sistema Nacional de Empleo . com

Senior Clinical Research Associate



Senior Clinical Research Associate – Homebased (Madrid, Valencia, Barcelona)

Josh Zarembski is delighted to offer a brand new opportunity to be part of a new and expanding clinical team based in Spain!

With just over 500 people working globally, this mid-size CRO is looking for a dedicated Senior CRA to help assist with normal day-to-day CRA tasks while also assisting the Clinical Trial Manager & Project Manager with additional responsibilities.

You will have the chance to enhance your career and gain the needed experience to break into the next stage of your career with support and training from industry-leading professionals.

This CRO pride itself on its enjoyable working environment. You will have the chance to work on and manage in-depth studies and develop your understanding in all areas!

Clinical Research Associate responsibilities will be in the areas of:

  • Responsible for collection and assessment of essential documents and perform reconciliation of Investigator
  • Site File. Conduct pre-study visits, site initiation visits, site monitoring visits and site closeout visits.
  • Assesses IP accountability, dispensation, and compliance at the investigative sites.
  • Prepare accurate and timely visit reports in accordance with the monitoring plan and/or SOPs.
  • Demonstrates working knowledge of applications and Systems (e.g. CTMS, eTMF, IVRS/IWRS and EDC).
  • Facilitates site audits and audit finding resolutions.
  • May supervise work of, or mentor, less experienced CRAs.
  • Serve as an observational visit leader.
  • Provide feedback to management and cross-functional study team on any current or potential risks or problems affecting the conduct of the clinical trial.
  • Feedback on any areas requiring improvement within the department and involvement in initiatives such as updating SOPs, Work instructions and Processes.
  • Can be involved in other tasks as assigned by Management, CTLs and PMs.
The experience required
  • Degree within Life Sciences or relevant Experience with independent monitoring, within a Pharma/CRO setting, for 3 + years
  • Previous experience in different types of monitoring
  • Ability to travel
  • Valid driver’s license
AL Solutions are a niche Life Science recruitment consultancy. We place professionals across the UK/EU for a variety of biotechnology, pharmaceutical and CRO companies ranging from small start-ups to large global organisations.

Josh Zarembski

AL Solutions




Fecha de publicación: 22/10/2022

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