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Company Description:
- Medicine moves forward here. Clinical trials, safety studies, and audits make safe and innovative pharmaceutical-led care possible.
- As part of Ergomed Group, you help patients benefit so they experience more of life’s meaningful moments. Biopharmaceutical companies are our clients, patients are our purpose.
Job Description:
- 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 and supports preparation of regulatory and/or EC submissions.
Qualifications:
- College/University degree in Life Sciences or equivalent combination of education, training & experience.
- Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials in oncology or rare disease.
- Full working proficiency in English and ability to plan, multitask and work in a dynamic team environment.
Ergomed Group
Ergomed Group is a clinical research organization (CRO) that helps biopharmaceutical companies develop, deliver, and safeguard therapies in oncology, rare disease, and other complex areas. The company fosters a culture of kindness, curiosity, and a shared sense of purpose, with a diverse team of experts in clinical research, pharmacovigilance, and quality consulting.