College/University degree in Life Sciences or equivalent experience
Extensive on-site monitoring experience in phase 2/3 trials, particularly in oncology or rare diseases
Full working proficiency in English
Strong planning and multitasking abilities in a dynamic team environment
Excellent communication, collaboration, and problem-solving skills
Willingness to travel nationally
Responsibilities
Conduct on-site or remote monitoring visits to ensure investigational site readiness
Verify investigator qualifications and site resources throughout the study
Train site staff as needed to ensure compliance and efficiency
Assist in preparing regulatory and ethics committee submissions when applicable
Mentor and train new staff, including performing co-monitoring visits to evaluate performance
Benefits
Join a passionate and collaborative team in clinical research
Contribute to bringing safe and effective treatments to patients globally
Work in an environment that values quality, integrity, and trust
Be part of a diverse workplace where every voice counts
Engage in a culture that emphasizes agility and responsiveness
Full Job Description
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
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
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 in oncology or rare disease
Full working proficiency in English
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
Ability to travel nationally
Additional Information
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.
