Study Start Up Associate I - Remote

Overview

The Study Start Up Associate I at ICON plays a crucial role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.

In Short

• Assist in preparation and submission of regulatory documents.
• Coordinate with stakeholders for study initiation approvals.
• Maintain records of regulatory submissions and approvals.
• Support study teams in developing study documents.
• Participate in study start-up meetings.
• Contribute to regulatory requirements and timelines.
• Work independently and manage multiple tasks.
• Foster collaboration with cross-functional teams.
• Emphasize attention to detail and organizational skills.
• Engage in a diverse and inclusive work environment.

Requirements

• Bachelor's degree in life sciences or related field.
• Previous experience in clinical research or regulatory affairs preferred.
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal skills.
• Ability to work independently.
• Capability to manage multiple tasks simultaneously.
• Work in a fast-paced environment.

Benefits

• Competitive salary and diverse culture.
• Various annual leave entitlements.
• Health insurance offerings for you and your family.
• Competitive retirement planning offerings.
• Global Employee Assistance Programme.
• Flexible country-specific optional benefits.
• Support for well-being and work-life balance.