Clinical Trial Coordinator

Veritus Research; Melbourne; On-site; AUD 65,000 - 95,000; Full time

Job summary

Veritus Research in Melbourne, Australia, is seeking an experienced Clinical Trials Coordinator (I or II) to join our Project Delivery Team at our state-of-the-art Clinical Research Unit. The role involves coordinating and managing multiple early-phase trials, ensuring protocol and ethical guideline compliance.

You will maintain source documentation and data entry, liaise with Principal Investigators and trial monitors, and contribute to the team’s drive for high-quality trial conduct.

Qualifications

• At least 2 years experience in Clinical Trials.
• Tertiary qualification in Science, Life Sciences, Nursing, Pharmacy or equivalent working experience desirable.
• Australian Citizen, Permanent Resident, or appropriate work visa.

Responsibilities

• Coordinate and manage a number of early-phase trials concurrently, ensuring compliance with the trial protocol and ethical guidelines.
• Ensure accurate source documentation and data entry, and maintain essential documents that validate trial conduct.
• Liaise with Principal Investigators, multidisciplinary team and trial Monitors.

Skills

Clinical Trials

Data entry

Documentation

Education

Tertiary qualification in Science/Life Sciences/Nursing/Pharmacy

Job description

Are you an experienced Clinical Trials Coordinator (I or II) looking for a change?

Do you want to join a dynamic team in a company that really values their staff?

If you said “Yes please!”, then get in touch as Veritus Research is looking for either an experienced CTC I or II (dependent on experience) to join our dynamic Project Delivery Team at our state-of-the-art Clinical Research Unit.

The successful applicant will work in a team environment with our Clinical, Medical, Pharmacy and Quality teams in a company that really values their staff.

So, if you want to help make our vision a reality for even more people, you will successfully:

Coordinate and manage a number of early-phase trials concurrently, ensuring compliance with the trial protocol, reporting requirements and ethical guidelines.

Exceed our Sponsor and CRO expectations by ensuring accurate and timely source documentation and data entry, and the maintenance of essential documents that validate integrity in the conduct of the clinical trial.

Liaise with Principal Investigators, multidisciplinary team and trial Monitors.

Working at Veritus Research means that you join a team of committed, driven and highly-engaged individuals who work together to achieve our strong company goals.

We recognise the individual and collective achievements of our team and celebrate our wins together.

Demonstrate detail, drive, resilience and optimism in your daily practice.

Build rapport with your peers, colleagues and key stakeholders.

Take personal responsibility trial conduct and the details of each project you are involved in.

Use innovation to tackle obstacles and achieve business growth and goals.

And whether you have the skills and qualifications like:

At least 2 years experience in Clinical Trials

Tertiary qualification in Science, Life Sciences, Nursing, Pharmacyor equivalent working experience desirable (or equivalent working experience)

Australian Citizen, Permanent Resident, or appropriate work visa