Clinical Research Associate I/II

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.

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.