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.
- 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.
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.