Clinical Trials Associate at ICON Strategic Solutions
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You will be responsible for coordinating clinical trials, ensuring adherence to protocols, and supporting cross-functional team collaboration. With a background in clinical research, your expertise will help maintain essential documentation and facilitate the development of new treatments for patients.
Key Responsibilities:
• Coordinate and administer clinical trials ensuring protocol compliance
• Organize study files and regulatory documents
• Prepare materials such as informed consent and case report forms
• Work with teams to ensure smooth trial execution
• Track and report on trial metrics and milestones
Requirements:
• Bachelor’s degree in a relevant field
• Two years of clinical research experience needed
• Familiarity with regulatory documentation
• Oncology knowledge is essential
• Excellent organizational and communication skills
Contribute to valuable clinical research processes aimed at advancing oncology treatments through your role at ICON.
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