Job Overview
The Clinical Research Associate 1 role is pivotal in ensuring the success of our studies.
Key Responsibilities:
* Engage in site visits to monitor every aspect of the study, from regulatory submissions to data query resolutions.
* Develop and implement innovative recruitment strategies to recruit study subjects.
* Empower sites with knowledge by providing essential training and maintaining robust communication channels.
* Champion quality and integrity by evaluating and enhancing site practices.
* Drive study progress by monitoring every aspect of the study.
Requirements:
* A degree in life sciences or healthcare (or equivalent experience).
* 12 months minimum on-site independent monitoring experience, preferably in haematology.
* Deep knowledge of GCP, ICH, and clinical trial operations.
* Tech-savvy with Microsoft Office and mobile tools.
* A proactive mindset, strong communication skills, and a passion for excellence.
Why Choose This Opportunity?
* Work on diverse, global studies across multiple therapeutic areas.
* Be part of a supportive, innovative team that values your growth.
* Enjoy flexible work arrangements, travel opportunities, and career development.