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 in Barcelona or Madrid
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.
- Support regulatory team in preparing documents for study submissions.
- College/University degree in Life Sciences or an equivalent combination of education, training & experience.
- Clinical Research or Medical experience.
- Full working proficiency in English and Catalan.
- PC skills to be able to work with MS Word, Excel and PowerPoint.
- Ability to plan, multitask and work in a dynamic team environment.
- Communication, collaboration, and problem-solving skills.
- Ability to travel.
Become a full-fledged clinical research professional with the support of a knowledgeable and professional team. You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.
