SCRA, Spain

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.

Responsibilities:

• 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.

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