Overview
National Travel Required
Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study.
Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment, and staff to conduct the clinical study throughout the study period.
Trains investigational site staff as necessary.
When applicable, supports preparation of regulatory and / or EC submissions.
Participates in mentoring / training of new staff as well as performing co-monitoring visits to assess junior staff performance.
Qualifications
Why Ergomed
We prioritize diversity, equity and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
To succeed we must work together with a human first approach. Why because our people are our greatest strength leading to our continued success on improving the lives of those around us.
Benefits
Training and career development opportunities internally
Strong emphasis on personal and professional growth
Friendly supportive working environment
Opportunity to work with colleagues based all over the world with English as the company language
Our core values are key to how we operate and if you feel they resonate with you then Ergomed is a great company to join!
We look forward to welcoming your application.
Remote work : Full-time
Key Skills : CSS, Cloud Computing, Health Education, Actuary, Building Electrician
Experience : years
Vacancy : 1
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Clinical Research Associate Ii • madrid, España