About the Position
We are seeking a highly skilled Clinical Research Associate Specialist to join our global clinical research organisation. This is an excellent opportunity to work in a dynamic environment driven by innovation and continuous improvement.
Your Key Responsibilities
You will be responsible for performing all aspects of CRA duties from site selection to database lock, including:
* Site selection, initiation, and routine monitoring visits
* Close-out visits and database lock
In addition, you will oversee all aspects of study site management to ensure high-quality data and consistently low query levels. You will also support and mentor other team members.
What We Are Looking For
We are looking for an individual with:
* A degree in Pharmacy or a related field
* At least 2+ years of prior monitoring experience with global trials
* Strong Oncology monitoring experience
* Excellent communication skills
* Excellent knowledge of international guidelines (ICH-GCP) and local regulations
Our Offerings
We provide a competitive salary, a range of additional benefits, and opportunities for career growth and development. Our benefits include:
* Annual leave entitlements
* Health insurance offerings
* Competitive retirement planning options
* Employee Assistance Programme
* Life assurance
* Flexible country-specific optional benefits
We value inclusion, belonging, and diversity, and we are committed to providing an inclusive and accessible environment for all candidates.