Clinical Research Associate I

As a Clinical Research Associate I you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.

Office-based in Barcelona, Spain

You will:

• Conduct and report all types of onsite monitoring visits.
• Be involved in study startup.
• Perform CRF review, source document verification and query resolution.
• Be responsible for site communication and management.
• Be a point of contact for in-house support services and vendors.
• Communicate with internal project teams regarding study progress.
• Participate in feasibility research.

• College/University degree in Life Sciences.
• Minimum of 1 year of experience as a Study Coordinator, or
• At least 6 months of experience as a Clinical Research Associate.
• Full working proficiency in English and Spanish.
• Fluent in Catalan.
• Proficiency in MS Office applications.
• Ability to plan, multitask and work in a dynamic team environment.
• Communication, collaboration, and problem-solving skills.
• Ability to travel. 

What We Offer:

• Stability, long-term cooperation
• Permanent contract, full-time job
• Competitive salary and benefit package
• Career development 
• Unique combination of team collaboration and independent work
• Friendly and supportive colleagues
• Onboarding courses about clinical research industry
• Comfortable and well-established office

Make the right call and take your career to a whole new level.  Join the company that focuses on its people and invests in their professional development and success.