Clinical Research Associate I/II

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.