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Want to work for an organisation that encourages you to shape, foster, consider the unorthodox approach and believe wholeheartedly in what you do? Come and join our Team.

At Emeritus Research, we believe that it is the ability of our people that makes us so good at what we do. Every member of our Team has the drive to make a difference to the lives of our patients, each and every day. They are motivated by personal satisfaction of a job well done, always striving to deliver clinical research in ever-superior ways. At the heart of it, we create health-related change for the better. This is why we love what we do.

We have a strong history of success at Emeritus Research but we are more then ready to branch out in new ways. If you’re keen to help us establish our future direction and put Emeritus Research on the map, please get in touch today.

See our Current Vacancies below:

 

Senior Clinical Research Coordinator/Project Manager

Do you have clinical trial experience? Keen to give up regular work travel? Interested in a project management role at a research site?

The Senior CRC/PM will be responsible for HREC submissions, scheduling and conducting trial assessments, managing clinical trial supplies and recruitment activities, data collection activities and financial and operational status reporting. Communicating with Sponsor and CRO representatives is an important part of the role so excellent relationship management skills are needed. Attention to detail is critical and your first-rate clinical and assessment skills should be complimented by the ability to maintain high quality source documents. The Senior CRC/PM role is an autonomous one and as you will be working in a busy environment with a number of competing priorities, being able to proactively manage your workload and thrive under pressure are a must.

Standard office hours are 7.30am to 4.30pm, although there may be the occasional earlier start or later finish depending on individual trial requirements. We offer generous financial packages for the right people including access to an Accrued Day Off (ADO) program. This role is a permanent position and full or part-time hours will be considered.

Qualifications, Attributes & Experience:

  • Degree qualified in nursing, science or allied health
  • +3 years experience in clinical trials
  • +2 years patient-focused clinical experience
  • Proficient in Microsoft Office
  • Previous exposure to clinical trial finances
  • Australian citizen or have permanent residency in place
  • Senior CRAs, Project Managers and/or applicants with prior CRO experience would be very highly regarded

 

 

Clinical Research Coordinator

Are you a Registered Nurse? Do you have experience or an interest in running clinical trials? Keen to give up shift work?

The CRC will be responsible for scheduling participant visits, conducting trial assessments in conjunction with our Principal Investigators, managing clinical trial supplies and recruitment activities, data collection activities and status reporting. Communicating with Sponsor and CRO representatives is an important part of the role so excellent relationship management skills will be needed. Attention to detail is critical and your first-rate clinical and assessment skills should be complimented by the ability to maintain high quality source documents. The CRC role is an autonomous one and as you will be working in a busy environment with a number of competing priorities, being able to proactively manage your workload and thrive under pressure are a must.

Standard office hours are 7.30am to 4.30pm, although there may be the occasional earlier start or later finish depending on individual trial requirements. We offer generous financial packages for the right people including access to an Accrued Day Off (ADO) program. This role is a permanent position and full or part-time hours will be considered.

Qualifications, Attributes & Experience:

  • Degree qualified with APHRA Registration
  • +5 years clinical nursing experience
  • Proficient in Microsoft Office
  • Clear understanding of the clinical research process
  • Australian citizen or have permanent residency in place
  • Candidates with direct clinical research, clinical trials or medical research as well as eDC experience will be highly regarded