Job Overview
We are seeking a highly skilled and experienced Setup Specialist to join our team. In this role, you will play a pivotal part in coordinating the initial stages of clinical trials, ensuring all operational and logistical elements are in place for successful execution.
Key Responsibilities
* Coordinate the setup of clinical trials, including site selection, regulatory document preparation, and study material distribution.
* Collaborate with cross-functional teams to ensure alignment on study protocols, timelines, and operational requirements.
* Ensure compliance with Good Clinical Practice (GCP) and other regulatory guidelines throughout the study setup phase.
Requirements
To be successful in this role, you will need:
* A bachelor's degree in a relevant field such as life sciences, clinical research, or healthcare management.
* Experience in clinical trial setup, regulatory submissions, or site management, preferably within the pharmaceutical or biotechnology industry.
* Strong understanding of clinical trial processes, regulatory requirements, and GCP guidelines.
Benefits
We offer a range of benefits to support your well-being and work-life balance, including:
* Various annual leave entitlements.
* A range of health insurance offerings to suit your needs.
* Competitive retirement planning options.
Inclusion & Belonging
We are committed to providing an inclusive and accessible environment for all candidates. We welcome applications from diverse backgrounds and are dedicated to fostering a culture of inclusion and belonging.