Clinical Research Associate II

Benefits

Additional Information

As a CRA 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, Spanish and 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

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