Regulatory Affairs Assistant - Bogota, Colombia - PSI CRO
Descripción
Company Description
We are the company that cares - for our staff, for our clients, for our partners and for the quality of work we do.
Job Description:
Join our international team and support regulatory aspects of clinical research projects, streamlining communication, maintaining electronic systems and managing documents.
- Home-Based position in Colombia._
- Only CVs in English will be considered._
You will:
- Be the point of contact for clinical project teams and support services on regulatory matters;
- Prepare draft regulatory/ethics submission dossier;
- Be responsible for document management such as filing, processing, translation, quality control;
- Update and maintain (automated) tracking systems, working files, and schedules;
- Organize meetings, prepare agendas and minutes;
- Perform trainings of PSI clinical research staff in the departmental software.
Qualifications:
- College/University degree or an equivalent combination of education, training & experience;
- Life Science degree is a plus;
- Administrative work experience, preferably in an international setting is a plus;
- Prior experience in Clinical Research is a plus;
- Full working proficiency in English and Spanish;
- Ability to plan and work in a dynamic team environment;
- Communication and collaboration skills.
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.
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