Senior CRA / CRA II - Home Based - Barcelona

• Be responsible for the successful conduct of clinical trials
• International Company with Career Progression

International CRO Company especialized in Clinical Trials and Consulting, present in America, Europe and Asia.

• Conduct qualification, initiation, monitoring and close the visits.


• Provide ongoing updates and support to project management


• Ensure clinical data integrity and meet study timelines.


• Assist with regulatory and study start-up activities including contract and budget negotiations.


• Attend global project meetings including investigator meetings and global team teleconferences.


• Complete assigned training programs in drug development processes, therapeutic areas, Good Clinical Practices (GCPs) and any applicable local regulatory requirements.


• May serve as mentor / trainer for CRAs; may include conducting training/assessment visits.


• May function in the role of Lead CRA for assigned project(s).

• Permanent and Full time (40h/week) position.


• Conditions according to candidate experience.


• Meal card: allowance of 11€/worked day.


• Medical Insurance for the employee and family.


• Life Insurance.


• 25 vacation days + n.º of days stipulated on the CBA.


• Possibility of Car allowance.

• Life science Degree. Monitoring MSc will be a plus.


• At least 3 years of clinical research experience as a CRA or related role.


• Excellent knowledge: ICH-GCP and regulatory.


• Fluent in Local Language and English (both oral and written).