About this role
National Travel RequiredPerforms 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 studyIdentifies 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 necessaryWhen applicable, supports preparation of regulatory and / or EC submissions College/University degree in Life Sciences or an equivalent combination of education, training & experienceExtensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials such as oncology / rare disease Full working proficiency in English and FrenchAbility to plan, multitask and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travel When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.
Quality: we hold ourselves to the standard patients deserve.Integrity and trust: we do the right thing, especially when it is hard.Drive and passion: we care about the outcome, because someone is waiting on it.Agility and responsiveness: we move quickly, because patients cannot wait.Belonging: everyone is welcome, and every voice counts.Collaborative partnerships: we go further by going together.We look forward to welcoming your application