About the role
Job Description
As a Clinical Research Associate I 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. You will focus on subjects’ rights, safety and well-being and quality of data compliance.
Office-based / Hybrid in Barcelona, Spain
You will:
* Conduct and report all types of onsite monitoring visits. * Be involved in study startup. * 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.
Qualifications
* College/University degree in Life Sciences. * Minimum of 1 year of experience as a Study Coordinator, or * At least 6 months of experience as a Clinical Research Associate. * Full working proficiency in English and Spanish. * Fluent in 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.
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.