Clinical Trial Doctor

Evolve Scientific an NES Fircroft Company; Sydney; Sur place; AUD 150 000 - 190 000; Plein temps

Avantages offerts par ce poste

Flexible working arrangements

Clear progression pathway

Industry-sponsored clinical trials

Supportive multidisciplinary research

Résumé du poste

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.

Responsabilités

• 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.

Connaissances

ICH-GCP knowledge

Clinical trial coordination

Participant safety

Data integrity

Regulatory compliance

Formation

Unrestricted AHPRA registration

Description du poste

Clinical Trial Investigator (Principal Investigator / Sub-Investigator)

Full-Time | 0.8 FTE | 0.6 FTE (Part-Time Options Available)

Are you an experienced Principal Investigator, or a Medical Doctor ready to step into a Sub-Investigator role with a clear pathway toward Principal Investigator responsibilities?

An rare and exciting opportunity is available at a well-established clinical research site, part of a high-performing research network delivering patient-focused, industry-sponsored trials across diverse therapeutic areas. This role is ideal for clinicians passionate about clinical research and eager to contribute to innovative studies within a supportive and collaborative environment.

About the Role

As a Clinical Trial Investigator, you will play a key role in the successful delivery of clinical trials, ensuring the highest standards of patient care, safety, and protocol compliance.

Key responsibilities include:

• Leading or supporting the conduct of clinical trials in accordance with ICH-GCP, regulatory requirements, and site SOPs
• Performing protocol-specific procedures including medical assessments, laboratory result interpretation, ECG review, and imaging evaluation
• Obtaining informed consent and maintaining ongoing participant safety and engagement
• Providing medical oversight of trial participants, ensuring data integrity and protocol adherence
• Collaborating closely with investigators, study coordinators, and site staff
• Supporting quality improvement initiatives and implementation of clinical best practices
• Working alongside site operations to ensure efficient, compliant study execution

About You

We are seeking motivated and adaptable Medical Practitioners committed to advancing their careers in clinical research.

You will bring:

• Unrestricted registration with Australian Health Practitioner Regulation Agency
• Experience as a Principal Investigator or Sub-Investigator or a strong desire to transition into a Sub-Investigator role
• Solid understanding of ICH-GCP and clinical trial processes
• Experience in commercially sponsored trials (highly regarded)
• Confidence in managing study participants and complex clinical protocols
• Strong organisational and time management skills
• A collaborative mindset with commitment to high-quality research outcomes

Why Apply?

• Flexible working arrangements (full-time, 0.8 FTE, or 0.6 FTE)
• Clear progression pathway from Sub-Investigator to Principal Investigator
• Opportunity to work on cutting-edge, industry-sponsored clinical trials
• Supportive, multidisciplinary research environment
• Exposure to diverse patient populations and therapeutic areas