As a Clinical Research Associate II, 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. Your focus will be on subjects' rights, safety and well-being and quality of data compliance. You will:

Conduct and report SIV, RMV, COV onsite monitoring visits

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

Support regulatory team in preparing documents for study submissions

Prepare and participate on audits and inspections

Requirements:

A degree in Life Sciences and a Master's degree in Clinical Trials are required





At least 1 year of independent on-site monitoring experience in Spain

Experience in all types of monitoring visits in Phase II and/or III

Full working proficiency in English and Spanish

Proficiency in MS Office applicationsAbility 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.

📌 Clinical Research Associate Ii (Madrid)
🏢 Psicro
📍 Madrid