Clinical Trials Start-Up Associate I — Remote/Hybrid

Icon; Australia; Hybride; AUD 70 000 - 95 000; Plein temps

Avantages offerts par ce poste

Annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Program

Life assurance

Country-specific benefits

Résumé du poste

ICON Strategic Solutions Australia is seeking a Study Start Up Associate I to help initiate clinical trials, ensuring regulatory compliance and contributing to patient-focused therapies. This role supports site activation, coordinating with stakeholders and preparing regulatory documents while maintaining meticulous records.

You will work with cross-functional teams, develop study materials, and participate in start-up meetings.

Qualifications

• Bachelor's degree in life sciences or related field.
• Experience in clinical research or regulatory affairs preferred, but not required.
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and manage multiple tasks in a fast-paced environment.
• Willingness to travel approximately 5%.

Responsabilités

• Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.
• Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
• Maintaining accurate and up-to-date records of regulatory submissions and approvals.
• Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures.
• Participating in study start-up meetings and providing input on regulatory requirements and timelines.

Description du poste

ICON Strategic Solutions Australia is seeking a Study Start Up Associate I to help initiate clinical trials, ensuring regulatory compliance and contributing to patient-focused therapies. This role supports site activation, coordinating with stakeholders and preparing regulatory documents while maintaining meticulous records.

You will work with cross-functional teams, develop study materials, and participate in start-up meetings.