Clinical Research Manager – Orthopedics Trials

Antler; Sydney; On-site; AUD 150,000 - 190,000; Full time

Benefits offered by this job

Competitive remuneration

Continuous training

Flexible working arrangements

Job summary

Johnson & Johnson in North Ryde, Australia is recruiting a Manager, Clinical Research to lead planning, execution, and oversight of clinical studies in orthopedics. The role partners with R&D, Medical Affairs, Regulatory and Quality to ensure scientifically sound and compliant programs that drive patient outcomes and product development.

You will manage site identification, feasibility, vendor relationships, start-up, monitoring, and CAPA processes, while aligning timelines and budgets across

Qualifications

• Bachelor’s degree required in life sciences or related.
• 6–8 years in clinical research or clinical operations.
• Experience leading cross-functional clinical studies.
• Strong knowledge of GCP and regulatory requirements.
• Excellent written and verbal communication.

Responsibilities

• Lead end-to-end clinical study operations across assigned programs.
• Drive site identification and feasibility assessments.
• Ensure studies comply with GCP and regulations.
• Serve as primary operations contact with cross-functional stakeholders.
• Develop and maintain operational study plans and budgets.
• Oversee monitoring resourcing and CRO coordination.
• Support inspections and CAPA processes.
• Coordinate global team communications across time zones.

Skills

Clinical operations lead

GCP knowledge

Cross-functional teamwork

Documentation skills

Stakeholder management

Education

Bachelor’s degree in Life Sciences

Advanced degree preferred

Tools

CTMS

Contract management

Budgeting

Project management

Job description

Johnson & Johnson in North Ryde, Australia is recruiting a Manager, Clinical Research to lead planning, execution, and oversight of clinical studies in orthopedics. The role partners with R&D, Medical Affairs, Regulatory and Quality to ensure scientifically sound and compliant programs that drive patient outcomes and product development.

You will manage site identification, feasibility, vendor relationships, start-up, monitoring, and CAPA processes, while aligning timelines and budgets across