Senior Clinical Research Associate — Hybrid (Sydney)

Novotech Global; Sydney; Hybrid; AUD 85,000 - 125,000; Full time

Job summary

Novotech Global is seeking a Clinical Research Associate (CRA) to safeguard trial participant rights and ensure data quality across source documents. The CRA serves as the primary contact between Investigational Sites, Novotech and Sponsors, overseeing site relationships and adherence to ICH GCP and SOPs.

Based in Sydney with hybrid working arrangements and flexible hours, this role requires strong time management, teamwork, and attention to detail to support timely trial delivery and regulatory

Qualifications

• Graduate in clinical or life sciences-related field.
• Experience in research or pharmaceutical industry preferred.
• Unrestricted working rights in Australia; visa sponsorship not available.
• Strong time management, attention to detail, teamwork and computer literacy.

Responsibilities

• Build relationships with Principal Investigators, study coordinators, pharmacists and site personnel to ensure efficient management of trials.
• Foster internal and external customer relationships to ensure timely project delivery per study requirements.
• Collaborate with IHCRA and RSA, prepare site essential documents and support ethics/regulatory submission processes as needed.
• Understand local and international regulatory requirements relevant to specific trials.
• Ensure recruitment of participants per site targets and support recruitment planning.
• Monitor investigational sites across all ICH GCP monitoring visit types (Site Selection, Initiation, Monitoring, Close Out).

Skills

Time management

Attention to detail

Teamwork

Computer literacy

Education

Graduate in clinical or life sciences

Job description

Novotech Global is seeking a Clinical Research Associate (CRA) to safeguard trial participant rights and ensure data quality across source documents. The CRA serves as the primary contact between Investigational Sites, Novotech and Sponsors, overseeing site relationships and adherence to ICH GCP and SOPs.

Based in Sydney with hybrid working arrangements and flexible hours, this role requires strong time management, teamwork, and attention to detail to support timely trial delivery and regulatory