CRA II/SCRA

An international contract research organisation (CRO) is advertising a vacancy for a CRA II/SCRA position. The company, which provides drug discovery, lifecycle management, and laboratory services is seeking for a driven and talented individual to join their company's office in Barcelona. This is an exciting opportunity to work with a company that provides innovative ideas behind multiple pharmaceutical sectors.

Job Responsibilities:

• Performing and coordinating all aspects of the clinical monitoring and site management process for company assigned sites in accordance with ICH GCP, local regulations, and PPD SOPs.
• Conducting conduct site visits to assess protocol and regulatory compliance.
• Managing required documentation to ensure that data will pass international quality assurance audits.

Skills and Requirements:

• Bachelor's degree in a life-science field.
• Previous clinical trial monitoring experience equivalent to 1 year or more in a CRA role.
• Proficiency in both English and Spanish.
• Demonstrable multitasking, project management, and execution skills.
• Good interpersonal skills, including communication, presentation, persuasion, and influence.
• Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
• Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Theodora Savlovschi-Wicks at +44 203 752 0314 or upload your CV on our website - www.Proclinical.com.

A full job description is available on request.

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

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