As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies
Job Summary
As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.
ICON offers a range of benefits focused on well-being and work-life balance, including various annual leave entitlements, health insurance options, retirement planning, and a global employee assistance program.
ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to a workplace free of discrimination and harassment.
Matching Summary
As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.
Skills & Requirements
Must-have
Regulatory document preparation and submission
Clinical trial start-up coordination
Regulatory compliance management
Project management skills
Cross-functional team collaboration
Nice-to-have
Process improvement initiatives
Inclusive and diverse work environment
Excellent communication skills
Key Requirements
Bachelor's degree in life sciences or related field
Minimum 2 years clinical research or regulatory affairs experience
Experience in study start-up activities
Knowledge of ICH-GCP and local regulatory requirements