We are seeking an experienced Clinical Research Associate to join our global team.
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About the Role
The successful candidate will perform all aspects of CRA duties, including site selection, initiation, routine monitoring visits, and close-out visits. This will involve managing all aspects of study site management to ensure high-quality data, low query levels, and good Quality Assurance reports.
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Responsibilities
* Perform all aspects of CRA duties, including site selection, initiation, routine monitoring visits, and close-out visits, leading to database lock.
* Manage all aspects of study site management to ensure high-quality data, low query levels, and good Quality Assurance reports.
Requirements
* Degree in Pharmacy or related field.
* At least 2 years of monitoring experience with global trials.
* Oncology monitoring experience is desirable.
* Excellent communication skills.
* Strong knowledge of international guidelines (ICH-GCP) and good understanding of local regulations.
* Flexibility to travel as needed.
Benefits
* Competitive salary and benefits package.
* Variety of annual leave entitlements.
* Health insurance options.
* Retirement planning options.
* Global Employee Assistance Programme (EAP) with 24/7 access to support professionals.
* Life assurance.
* Flexible country-specific benefits.
We offer a dynamic and supportive work environment that values innovation and collaboration. If you are a motivated and detail-oriented professional looking for a new challenge, we encourage you to apply.