Clinical Research Associate

ProClinical are advertising a Clinical Research Associate vacancy with a global Contract Research Organisation that offers fully integrated end-to-end clinical and commercial solution organisations. This company is seeking a new member for their Pairs based team to assist with clinical research projects in phases I-IV.

Job Responsibilities:

• Performing site qualification, monitoring, site initiation, site management and close out visits.
• Participating in study start-up.
• Performing CRF review, source document verification and query resolution.
• Overseeing site communication and management.
• Overseeing protocol compliance.
• Providing training and mentor ship to more junior CRAs.
• Supporting regulatory team in preparing documents for study submissions.

Skills and Requirements:

• Bachelor's degree in Life Sciences or an equivalent combination of education, training & experience.
• Strong experience in Oncology field.
• At least 2 years of independent on-site monitoring experience in France.
• Demonstrable experience in all types of monitoring visits.
• Proficiency in English and French.
• Communication, collaboration, and problem-solving skills.
• Ability to travel 75% of the time

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 call Sasha Brasero on +44 203 078 9556 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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