Clinical Research Associate

i‑Pharm Consulting; Sydney; On-site; AUD 90,000 - 130,000; Full time

Benefits offered by this job

Competitive salary package

Reduced travel requirements

Continuous professional development

Job summary

i-Pharm Consulting is seeking a Clinical Research Associate / Senior CRA in Australia. The role is based in Sydney & Brisbane, focusing on independent site monitoring and delivery of clinical trials within a collaborative CRO environment.

Join a team committed to excellence in clinical research, with opportunities for mentorship and professional development while maintaining a strong work-life balance.

Qualifications

• Bachelor's degree in Life Sciences, Nursing or related field.
• A valid Australian Driver's License.
• Minimum of 2 years' experience in a CRO environment with independent monitoring responsibilities.
• Proven experience in the Australian clinical research landscape.
• Full working rights in Australia (no overseas applicants).

Responsibilities

• Conduct and manage site monitoring activities independently, ensuring compliance with protocols, GCP and regulatory requirements.
• Develop and maintain strong relationships with site staff, investigators, and internal stakeholders.
• Oversee study progress, ensuring adherence to timelines and quality standards.
• Provide guidance and mentorship to junior CRAs as needed.

Skills

Site monitoring

Relationship building

Study oversight

Mentorship

Education

Bachelor's degree in Life Sciences / Nursing

Tools

Australian Driver's License

Job description

Job Title:

Clinical Research Associate / Senior Clinical Research Associate

Location:

Sydney & Brisbane

Join a Global CRO known for its personalised approach and commitment to excellence in clinical research. On offer is a collaborative environment where your contributions will make a significant impact.

• Competitive salary package
• Reduced travel requirements, allowing for better work-life balance
• Continuous professional development opportunities

The Opportunity:

We have an exciting full-time, permanent opportunity for an experienced Clinical Research Associate. You will play a key role in the successful delivery of clinical trials, working with a close-knit team of professionals who are passionate about advancing healthcare.

Key Responsibilities:

• Conduct and manage site monitoring activities independently, ensuring compliance with protocols, GCP, and regulatory requirements.
• Develop and maintain strong relationships with site staff, investigators, and internal stakeholders.
• Oversee study progress, ensuring adherence to timelines and quality standards.
• Provide guidance and mentorship to junior CRAs as needed.

Requirements:

• Bachelor's degree in Life Sciences, Nursing, or related field.
• A valid Australian Driver's License.
• Minimum of 2 years' experience in a CRO environment with independent monitoring responsibilities.
• Proven experience in the Australian clinical research landscape.
• Full working rights in Australia (Please note, we are unable to consider applicants from overseas).

This is your chance to be part of a company where you are valued as an individual, not just a number. the lower-than-average travel requirements mean more time for you to enjoy your personal life while still advancing your career in a supportive, engaging environment.