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. #J-18808-Ljbffr

📌 Clinical Research Associate II (Comunidad de Madrid)
🏢 Psicro
📍 Comunidad de Madrid