Cra

About the Role

We are seeking a highly skilled Senior Clinical Research Associate (CRA) to lead performance and compliance for assigned

protocols and sites within Scotland. Under the oversight of the CRA Manager or Clinical Research Director (CRD), you

will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to

ICH/GCP, local regulations, our company policies and procedures, quality standards, and adverse event reporting

requirements. You will take ownership of allocated sites, actively expand our clinical research territory by identifying

and developing new sites and contribute as a subject matter expert on monitoring processes and systems across internal

Responsibilities

• Perform core duties as described.

Requirements

• Relevant experience or willingness to learn.

Benefits

• Benefits per job description.

Compensation

To be discussed.

Location & Schedule

Per job description.

How to Apply

Use the “Apply” button.