Clinical Trial Coordinator

Clinical Trial Coordinator

• Are you looking for a change? 
• Have you got fabulous experience you want to share with a rapidly growing company with incredible vision?
• Want to work Monday-Friday and have your week-ends back? 
• Want 1 extra paid day off per month? 

If you said “Yes please!” to any of these, then get in touch as Emeritus Research is looking to add an amazing Clinical Trial Coordinator (CTC) who is ready to hit the ground running to our dynamic Clinical Trials Team in Camberwell.

We’ve already mentioned we have incredible vision - we improve world health by expertly managing clinical trials to accelerate medical advancements. By joining our team of energetic and passionate medical professionals, you will focus on improving patient outcomes helping us run over 50 trials in various specialties including Vaccines, Rheumatoid and Osteo arthritis, Gout, Cardiovascular and Mental health areas.

You don’t do this alone either. The CTC has great support working alongside and under the direction of a Team Leader and Principal Investigator, to support, facilitate and coordinate the daily trial activities of all our studies. The CTC ensures GCP (or good clinical practice) and protocol compliance, provides training of key personnel, actively participates in the recruitment of participants and works within the financial terms of the trial.

Do you want to work for a company that values their staff?

We’ve already mentioned full time staff get 1 extra paid day off per month; we also need to let you know the variety of snacks and fresh fruit in our kitchen are delicious. Plus over 90% of our staff agree Emeritus has an environment where team members with different backgrounds and styles work well together and individualism and originality is truly valued.

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

• Exceed our sponsor expectations by facilitating participant recruitment initiatives as we strive for our business goals
• Find solutions for any participant recruitment barriers 
• Meticulously ensure essential trial documents are maintained at a high standard 
• Efficiently manage all trial resources so everything you need is available for all participant visits
• Ensure sponsor expectations are fulfilled by having all data entry completed and queries attended to
• Put your eye for detail across all trials under your management to achieve great outcomes during internal financial, regulatory and source audits.

What’s next? Apply now and let us know how you:

• Constantly look for better ways of doing things and Improve processes and business outcomes.
• Thrive on success.
• Have a high level of Strategic Awareness ensuring that you constantly work towards the Sponsor and companies’ goals.
• Easily Build Rapport with others to establish comfortable working relationships with staff and Sponsors.
• Possess Drive, Resilience and Optimism to pursue your own, Sponsor and Emeritus Research goals, even during challenging times.
• Take Personal Responsibility for every facet of each project.
• Demonstrate Innovation approaching challenges in ingenious ways. 

And whether you have the skills and qualifications like:

• At least 2 years experience in a similar role
• Tertiary qualification in Science, Life Sciences, Nursing, Pharmacy
• Experience in clinical trials
• Australian Citizen, Permanent Resident, or appropriate work visa
• Current AHPRA Registration (where relevant)

We are looking forward to meeting you.