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

Employment type
Full-time

Work arrangement
Hybrid