Senior CRA / SCRA I — Remote Clinical Trials Lead

Avance Clinical Pty Ltd.; Australia; Remote; AUD 90,000 - 120,000; Full time

Benefits offered by this job

Flexible work options

Birthday day off

Job summary

Avance Clinical in Australia is seeking experienced CRA III / Senior CRA I to join our expanding Australian team. The role covers evaluation, initiation, monitoring and close-out of clinical trials to ensure compliance with SOPs, ICH GCP and regulatory requirements, working within a CRO environment.

You will conduct site feasibility, develop study documents, lead multi-site operations as Lead CRA, and mentor staff during co-monitoring visits, with travel up to 50%.

Qualifications

• Bachelor’s degree in life sciences, pharmacy, nursing or equivalent field.
• Formal CRA work experience in a CRO is expected (5+ years for SCRA).
• Must have ICH GCP training and knowledge of ICH GCP guidelines.

Responsibilities

• Conduct site and investigator feasibility activities.
• Develop study documents or plans under the supervision of the Study Project Manager.
• Lead multi-site monitoring as Lead CRA, including monitoring plan development and review of visit reports.
• Perform on-site and remote pre-study visits, initiation visits, dose witnessing visits, interim monitoring and close-out visits.
• Prepare and maintain high-quality site documentation and ensure compliance with protocol and regulatory requirements.
• Raise data queries, review CRFs and ensure timely resolution with site staff.

Skills

Communication skills

Problem solving

Teamwork under pressure

Travel readiness

Education

Bachelor’s degree in life sciences, pharmacy, nursing or equivalent field

Job description

Avance Clinical in Australia is seeking experienced CRA III / Senior CRA I to join our expanding Australian team. The role covers evaluation, initiation, monitoring and close-out of clinical trials to ensure compliance with SOPs, ICH GCP and regulatory requirements, working within a CRO environment.

You will conduct site feasibility, develop study documents, lead multi-site operations as Lead CRA, and mentor staff during co-monitoring visits, with travel up to 50%.