Clinical Trial Associate

Job summary

The Clinical Trial Associate will support the design and analysis of clinical trials, contributing to the development of new treatments and therapies. This role involves ensuring compliance with protocols and regulatory requirements while maintaining clinical trial documentation.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Prior experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced environment with attention to detail.
• Willingness to travel as required (approximately 10%).

Responsibilities

Rewards & Benefits

• Assist in coordinating and administering clinical trials, ensuring compliance with protocols and regulations.
• Maintain and organize clinical trial documentation, including study files and regulatory submissions.
• Support the preparation of study-related materials, such as informed consent forms and case report forms.
• Collaborate with cross-functional teams to facilitate communication and ensure smooth trial execution.
• Contribute to tracking and reporting of clinical trial metrics and milestones.
• Competitive base salary and performance-related incentives.
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.