Found Description
Ergomed is a full‑service CRO specializing in Oncology and Rare Disease.
Responsibilities
- Perform 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.
- Identify investigators and verify that the investigator has adequate qualifications, resources, facilities, equipment and staff to conduct the clinical study throughout the study period.
- Train investigational site staff as necessary.
- When applicable, support preparation of regulatory and / or EC submissions.
Requirements
National Travel Required.
Qualifications
- College/University degree in Life Sciences or an equivalent combination of education, training & experience.
- Extensive on‑site monitoring experience in phase 2/3 trials, ideally with experience of complex tri...