Role OverviewAs a Senior Clinical Research Associate, you will perform on-site or remote monitoring visit activities to ensure the conduct of clinical studies. You will identify investigators, train site staff, and participate in mentoring/training of new staff.
What You Will Do
Your day-to-day responsibilities will include performing Pre-Study, Initiation, Interim, and Close-Out monitoring visits, identifying investigators, training site staff, and supporting regulatory submissions.
Why It Might Be a Fit
This role requires extensive on-site monitoring experience in phase 2/3 trials, ideally with experience in complex trials in oncology or rare disease. You will be part of a collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
Requirements
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Extensive on-site monitoring experience in phase 2/3 trials
- 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
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