At a Glance
- Tasks: Lead and support clinical trials, ensuring patient care and protocol compliance.
- Company: Established clinical research site within a high-performing research network.
- Benefits: Flexible working arrangements and clear progression pathways.
- Other info: Collaborative environment focused on quality research outcomes.
- Why this job: Make a real impact in innovative clinical research with diverse patient populations.
- Qualifications: Medical degree with unrestricted registration and experience in clinical trials.
The predicted salary is between 82800 - 101200 $ per year.
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 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
Clinical Trial Doctor in Sydney employer: Evolve Scientific an NES Fircroft Company
Join a dynamic and supportive team at our brand-new clinical research site in Penrith, where you will have the unique opportunity to shape operations and enhance participant experiences from the ground up. We offer flexible working arrangements to promote work-life balance, alongside strong professional development and career progression opportunities in a collaborative environment focused on innovative clinical trials. This is an ideal role for those passionate about making a meaningful impact in healthcare while enjoying a stable and rewarding career path.
Contact Details:
Evolve Scientific an NES Fircroft Company Recruitment Team
