Clinical Research Associate II

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 • 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 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.