Job Summary
This is a challenging role for an experienced Clinical Research Associate to join our team.
About the Role
We are seeking a skilled and dynamic individual to partner with one of the world's premier Biopharmaceutical companies, working across a broad portfolio of medicines and vaccines. You will be responsible for performing all aspects of CRA duties from site selection through to database lock.
You will be fully embedded in the client's study team with a dedicated ICON line manager to support you. This will involve overseeing all aspects of study site management to ensure high-quality data resulting in consistently low query levels and strong Quality Assurance reports.
Key Responsibilities
* Perform site selection, site initiation, routine monitoring visits, close-out visits, and database lock.
* Be fully embedded in the client's study team with a dedicated ICON line manager.
* Oversee all aspects of study site management.
Requirements
* Degree in Pharmacy or a related field.
* 2+ years of on-site monitoring experience within CRO/Pharma/Biotech.
* Excellent communication skills.
* Adaptability to work in a dynamic environment.
* Good knowledge of ICH-GCP guidelines and local regulations.
* Flexibility to travel.
What We Offer
* Competitive salary.
* Variety of annual leave entitlements.
* Health insurance offerings.
* Competitive retirement planning offerings.
* Global Employee Assistance Programme.
* Life assurance.
About Us
We are committed to a diverse, high-performance culture that rewards talent and nurtures growth. If you are interested in this role but unsure if you meet all requirements, we encourage you to apply anyway.