Senior Study Start Up Associate

• 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

• Bachelor's degree in life sciences or a related field
• Previous experience in clinical research or regulatory affairs preferred, but not required
• Strong attention to detail and organizational skills
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams
• Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment

Experience in clinical research or regulatory affairs

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others