About the role
Job Description
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
Qualifications
* 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
Additional Information
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.