Clinical Research Job at Novotech Australia
Are you searching for a rewarding Clinical Research Job in a globally recognized CRO? This exciting Project Specialist role with Novotech offers life science graduates and early-career professionals a dynamic opportunity to grow within an international clinical development environment. If you are looking for Jobs in Australia that combine innovation, collaboration, and career progression, this could be your next big step in a global Clinical Research Job pathway.
About the Novotech
Novotech is a global Contract Research Organization (CRO) specializing in clinical development services across all therapeutic areas and trial phases. Headquartered in Sydney, the company operates 34 offices worldwide and employs over 3,000 professionals. With strong regulatory expertise and advanced therapeutic knowledge, Novotech partners with biotechnology and pharmaceutical companies to accelerate life-changing innovations to market. The organization promotes diversity, inclusion, flexible working arrangements, and continuous professional development.
Job Details:
- Job Title: Project Specialist
- Company: Novotech
- Job Identification: 3754
- Location: Level 19, 66 Goulburn Street, Sydney, New South Wales, 2000, Australia
- Employment Type: Full-Time
About the Role
The Project Specialist is a key member of the Project Support Team at Novotech. The role offers a defined professional career pathway for high-performing individuals and plays an essential part in supporting project execution within the clinical research environment.
Key Responsibilities
-
Assist Project Managers (PMs) in managing project deliverables, cost control, and risk management activities
-
Ensure the setup and ongoing maintenance of operational project plans, timelines, and study tracking tools and systems
-
Take a lead role in providing support services for regional studies
-
Coordinate closely with regional Clinical Support teams to ensure alignment and efficiency
Experience and Qualifications
-
Graduate qualification in a Clinical or Life Sciences–related field
-
Ideally 1–2 years of experience within the clinical research industry
-
Experience in pharmaceutical, CRO, or healthcare environments is advantageous
-
Previous experience in a Clinical Trial Administrator (CTA) role is highly regarded
-
Superior written and verbal communication skills
-
High proficiency in Microsoft Office and experience managing multiple databases
-
Excellent attention to detail with a strong focus on quality outcomes
-
Demonstrated ability to meet deadlines and manage high-volume workflows effectively
-
Proactive approach with a willingness to improve processes and address inefficiencies
-
Ability to work flexibly within a team and collaborate with internal and external stakeholders
Benefits in the Project Specialist Role:Â
Employees are supported with:
-
Flexible working arrangements
-
Paid parental leave for both parents
-
Flexible leave entitlements
-
Wellness programs
-
Ongoing professional development initiatives
