SCRA, Spain

€40000 - €50000 per annum
  1. Permanent
  2. Clinical Research Associate (CRA)
  3. Spain
Madrid, Spain
Posting date: 16 Nov 2023

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

Proclinical are recruiting for a SCRA, Spain to join a CRO. This role is on a permanent basis with the ability to work remotely from anywhere in Spain.


  • Handle and uphold information and documentation in CTMS, eTMF and numerous other systems as suitable and per timelines.
  • Recognise, examine and solve site performance, quality or compliance issues and raise as suitable in cooperation with clinical research lead and CRA line management.
  • Conduct both remote and on-site supervision and monitoring actions using numerous tools.
  • Gather, evaluate and oversee necessary regulatory documentation for study start-up, study maintenance and study close-out.
  • You will develop solid site relationships and guarantee consistent site relationships through all phases of the trial.
  • Acquire extensive comprehension of the study protocol and connected processes.
  • Arrange and handle numerous tasks, cooperating with any other internal roles to accomplish site promptness.
  • Partake in and contribute to on site selection and validation actions.
  • Other duties may be assigned to this role.

Key Skills and Requirements:

  • Educated to a degree level with demonstrable experience in a clinical research associate role or a mixture of education, training and experience.
  • Exhibited experience might be taken into consideration in place of education.
  • Familiarity with ophthalmic would be ideal.
  • Able to regularly examine protocol and GCP compliance.
  • Capable of comprehending how to properly examine an investigative site's abilities to performing clinical research.
  • Able to verify source data to reported data.
  • Capable of supervising and reporting on the progression of the trial from start-up to finish.
  • Expertise on how to select and qualify an investigative site.
  • A high attention to detail.
  • Know-how of reconciling and returning/destroying test article while performing initiation, interim and close-out visits.
  • Know-how of the federal guidelines governing research and the standards outlining GCPs.
  • Capacity to both read and exhibit an understanding of clinical research protocols as well as the importance of following the protocol.
  • Computer literacy.
  • Fluency in more than one language would be advantageous.
  • Leadership abilities with an intellectual curiosity.
  • An organised individual with an innovative attitude and the capacity to set objectives.
  • Able to resolve issues.
  • Keen on making a meaningful and purposeful impact.
  • Works well with others.
  • Willing to travel for business needs up to 75% of the time.

If you are having difficulty in applying or if you have any questions, please contact Carlos Rios at +44 203 148 8352.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.