Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities.
Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conducting the clinical study throughout the study period.
Trains investigational site staff as necessary.

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 trials.
Full working proficiency in English.

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.
We offer training and career development opportunities internally.
Strong emphasis on personal and professional growth.

Ergomed

Ergomed is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia. Our company allows for employee visibility, creative contribution and realistic career development.

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