Clinical Trial Investigator: Flexible Hours & PI Path

Evolve Scientific an NES Fircroft Company; Sydney; On-site; AUD 150,000 - 190,000; Full time

Benefits offered by this job

Flexible working arrangements

Clear progression pathway

Industry-sponsored clinical trials

Supportive multidisciplinary research

Job summary

Evolve Scientific, part of the NES Fircroft network, seeks a Clinical Trial Investigator (Principal Investigator or Sub-Investigator) to lead and oversee trials at a busy site in Sydney. You will ensure patient safety, regulatory compliance, and protocol adherence, with a clear pathway to PI responsibilities and flexible full-time or fractional hours (0.8 FTE or 0.6 FTE).

You will collaborate with investigators, study coordinators and site staff, contribute to industry-sponsored trials, and

Qualifications

• Unrestricted AHPRA registration is required.
• Strong understanding of ICH-GCP and trial processes.
• Experience in managing clinical trial participants and protocols.
• Experience in commercially sponsored trials is advantageous.
• Excellent organizational and time management skills.

Responsibilities

• Lead or support the conduct of clinical trials in line with ICH-GCP and site SOPs.
• Perform medical assessments, ECG review, and imaging evaluation as required.
• Obtain informed consent and ensure ongoing participant safety.
• Provide medical oversight and ensure data integrity and protocol adherence.
• Collaborate with investigators, coordinators and site staff to ensure quality trial delivery.
• Drive quality improvement initiatives and best practices in the site.
• Support efficient, compliant study execution with site operations.

Skills

ICH-GCP knowledge

Clinical trial coordination

Participant safety

Data integrity

Regulatory compliance

Education

Unrestricted AHPRA registration

Job description

Evolve Scientific, part of the NES Fircroft network, seeks a Clinical Trial Investigator (Principal Investigator or Sub-Investigator) to lead and oversee trials at a busy site in Sydney. You will ensure patient safety, regulatory compliance, and protocol adherence, with a clear pathway to PI responsibilities and flexible full-time or fractional hours (0.8 FTE or 0.6 FTE).

You will collaborate with investigators, study coordinators and site staff, contribute to industry-sponsored trials, and