Employer Industry: Clinical Research Organization

Why consider this job opportunity:
- Competitive salary with various annual leave entitlements
- Comprehensive health insurance offerings for you and your family
- Competitive retirement planning options to help you save for the future
- Access to a Global Employee Assistance Programme for personal well-being support
- Flexible benefits including childcare vouchers, gym memberships, and health assessments
- Opportunity to work in a diverse and inclusive environment that values innovation

What to Expect (Job Responsibilities):
- Coordinate compliance and operational tasks in support of the Document Review Committee process
- Facilitate the review process by assessing the readiness of research documents and ensuring adherence to timelines
- Address stakeholder questions regarding the review process and resolve issues promptly
- Participate in continuous improvement projects to enhance operational effectiveness
- Manage internal meetings, including drafting and reviewing agendas and minutes

What is Required (Qualifications):
- Bachelor's degree required; education in public health or closely related discipline preferred
- 1-3 years of relevant experience in real-world evidence studies, observational research, or related roles
- Proficient in Microsoft 365 applications (Word, PowerPoint, Excel, Teams, etc.)
- Strong communication (oral and written) and organizational skills
- Basic knowledge of epidemiologic or outcomes research

How to Stand Out (Preferred Qualifications):
- Master’s degree in public health or a research-related field such as epidemiology or health services research
- Strong project management skills with the ability to manage multiple deadlines
- Ability to work independently and demonstrate flexibility in a dynamic environment

#ClinicalResearch #ProjectManagement #DiversityAndInclusion #EmployeeBenefits #CareerOpportunity

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