Are you an experienced Clinical Research Associate (CRA) looking to accelerate your career with a globally recognized Clinical Research Organization (CRO)? Novotech is hiring Clinical Research Associate II and Clinical Research Associate III professionals to support innovative biotechnology and pharmaceutical clinical trials. This opportunity allows experienced CRAs to work on Early Clinical Development and Phase I-III clinical studies while collaborating with leading biotech sponsors.

If you have independent site monitoring experience, strong knowledge of ICH-GCP, and a passion for clinical research, this is an excellent opportunity to join one of the world’s fastest-growing CROs.

About Novotech

Novotech is a globally recognized full-service Contract Research Organization (CRO) specializing in clinical research and scientific advisory services for biotechnology and pharmaceutical companies.

Founded in 1997, Novotech has expanded to more than 30 offices across Asia-Pacific, Europe, and the United States, supporting sponsors in accelerating the development of life-changing therapies.

The company has been recognized as:

• Employer of Choice
• Great Place to Work
• Employer of Choice for Gender Equality

Job Details

Key Responsibilities

As a Clinical Research Associate, you will:

• Independently monitor assigned clinical trial sites.
• Ensure compliance with ICH-GCP guidelines and study protocols.
• Perform routine monitoring visits and follow-up activities.
• Build strong relationships with investigators and study coordinators.
• Support patient recruitment and site performance.
• Collaborate with Regulatory Start-Up teams and IHCRAs.
• Ensure participant safety throughout clinical trials.
• Verify clinical data quality and integrity.
• Communicate effectively with sponsors and internal stakeholders.
• Identify study risks and recommend proactive solutions.

Required Qualifications

Applicants should possess:

• Bachelor’s Degree in:
  • Pharmacy (B.Pharm)
  • Life Sciences
  • Nursing
  • Health Sciences
  • Related healthcare discipline

Experience Requirements

Clinical Research Associate II

• Minimum 6 months independent site monitoring experience

Clinical Research Associate III

• Minimum 2 years independent site monitoring experience

Required Skills

Candidates should have:

• Strong knowledge of ICH-GCP Guidelines
• Clinical Trial Monitoring
• Site Management
• Investigator Relationship Management
• Clinical Documentation
• Clinical Operations
• Communication Skills
• Problem Solving
• Risk Management
• Regulatory Compliance

Why Join Novotech?

Novotech offers an employee-focused workplace with excellent career growth opportunities.

Benefits include:

• Flexible working hours
• Hybrid work arrangements
• Career advancement opportunities
• Exposure to Early Phase and Phase I-III Clinical Trials
• Dedicated mentoring from experienced Clinical Operations leaders
• Collaborative and supportive work culture
• Employee wellbeing programs
• Global clinical research exposure
• Opportunity to work with leading biotech sponsors

Eligibility

Applicants must:

• Have unrestricted working rights in Australia
• Hold relevant CRA monitoring experience
• Meet educational requirements
• Be willing to work within Clinical Operations

Note: Visa sponsorship is not available for this position.

Why This Role is a Great Opportunity

This Clinical Research Associate position offers professionals the opportunity to work on cutting-edge biotechnology studies while expanding expertise in site monitoring, regulatory compliance, and global clinical operations.

Working with Novotech provides direct exposure to international sponsors, complex clinical trials, and structured career progression in one of the world’s leading CROs.

How to Apply

Application Link