Clinical Trial Coordinator - Emeritus Research - ResearchCareer

First listed on: 19 March 2024

Clinical Trial Coordinator

 

Clinical Trial Coordinator - Full time

Are looking for a change?

Would you like to work Monday-Friday and get your weekends back?

We are looking for a clinical trial coordinator for our Clinical Trials Team in Sydney, to join our rapidly expanding team.  

We are currently running over 15 trials in various specialties including Vaccines, Rheumatoid and Osteo arthritis, Gout, Cardiovascular and Mental health areas.

Emeritus Research improves world health by expertly managing clinical trials to accelerate medical advancements.

The Clinical Trial Coordinator (CTC) works alongside and under the direction of the Clinical Trial Team Leader and Principal Investigator (PI), to support, facilitate and coordinate the daily trial activities of all studies at Emeritus Research. They ensure GCP and protocol compliance, provide training of key personnel, actively participate in the recruitment of participants and work within the financial terms of the trial.

Are you interested in Clinical Trial research?

Emeritus Research improves world health by expertly managing clinical trials to accelerate medical advancements. Join our team of energetic and passionate staff and medical professionals focused on improving patient outcomes through world class clinical trials. We work with the top global Pharmaceutical and Biotechnology companies, and we have been part of many trials that brought today’s leading medications to market.

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

Over 90% of our staff agreed that Emeritus Research has created an environment in which staff from different backgrounds and styles can work well together and 80% of staff agreed that staff individualism and originality is valued.

To be successful in the role you will: 

  • Report 100% of Sponsor recruitment updates within 24 hours to the Clinical Trial Team Leader
  • Ensure e-ISF is up to date for 100% of monitoring visits, resulting in no filing gaps
  • Ensure trial resources are managed such that all necessary supplies are available for every patient visit, achieving 100% readiness.
  • 100% of data entry is completed and all EDC and monitoring queries are attended to within contract timelines
  • Ensure 100% of trials under your management have internal financial, regulatory and source audits completed quarterly.

To be considered for the role, you need to:

  • You constantly look for better ways of doing things and Improve processes and business outcomes.
  • You Thrive on success.
  • You 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.
  • Possession of Drive, Resilience and Optimism to pursue your own, Sponsor and Emeritus Research goals, even during challenging times.
  • You take Personal Responsibility for every facet of each project.
  • Demonstrated Innovation approaching challenges in ingenious ways. 

SKILLS AND QUALIFICATIONS

  • Tertiary qualification in Science, Life Sciences, Nursing, Pharmacy
  • Experience in clinical trials (desirable)
  • Australian Citizen, Permanent Resident, or appropriate work visa
  • Current AHPRA Registration (if applicable)

How to Apply 

Click the APPLY button and include your resume and cover letter. 

Please contact Fiona Kilkenny 02 8964 8186 if you have any questions.