Clinical Research Associate I/II

Psi CRO; Barcelona; On-site; EUR 28,000 - 36,000; Full time

Benefits offered by this job

Competitive salary

Team collaboration

Onboarding courses

Friendly and supportive colleagues

Well-established office

Job summary

PSI CRO is seeking a Clinical Research Associate I for its Barcelona office. You will lead onsite monitoring visits, oversee site relationships, and collaborate with project teams to ensure study timelines and data quality are met.

Qualifications include a Life Sciences degree, 6 months to 1 year of CRA/Study Coordinator experience, fluency in English and Spanish, and Catalan. Travel is required, and MS Office proficiency is essential for daily tasks.

Qualifications

• Bachelor’s degree in Life Sciences.
• 1 year of experience as a Study Coordinator, or 6 months as a Clinical Research Associate.
• Fluent in English and Spanish; Catalan fluency.
• Proficiency in MS Office applications.

Responsibilities

• Conduct and report onsite monitoring visits.
• Be involved in study startup.
• Perform CRF review, source data verification and query resolution.
• 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.

Skills

Multitasking

Communication

Collaboration

Problem solving

Travel flexibility

Education

Bachelor's degree in Life Sciences

Tools

MS Office

Job description

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.

Job Description

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.

Qualifications

• 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.

Additional Information

What We Offer:

• Competitive salary and benefit package
• 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.