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. PSI is a leading Contract Research Organisation with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.