Clinical Trial Associate

A biotech dedicated to advancing innovative oncology therapies is seeking a motivated Clinical Trial Associate (CTA) to support our clinical studies and enhance patient outcomes.

Position Overview:

As a CTA, you will assist in the planning, execution, and management of clinical trials, working closely with project managers and cross-functional teams to ensure smooth operations.

Key Responsibilities:

• Prepare and maintain trial-related documentation, including protocols and consent forms.
• Support the management of trial timelines, budgets, and resources.
• Coordinate site activities, including selection, initiation, monitoring, and close-out.
• Maintain study files and databases, ensuring compliance with regulatory requirements.
• Assist in training site personnel on study protocols.
• Monitor study progress and address any arising issues.

Qualifications:

• Bachelor’s degree in life sciences or a related field.
• 1-3 years of clinical research experience, preferably in oncology.
• Understanding of clinical trial processes and GCP regulations.
• Strong organizational skills and attention to detail.
• Proficient in Microsoft Office and clinical trial management systems.
• Excellent communication skills and team collaboration.