Clinical Research Coordinator

CRCMelb_1707285256
  • Melbourne, Victoria
  • Permanent

Are you seeking a new role in Clinical Research?

Here is a chance to join a unique clinical research business who are growing their team in Melbourne....

This company have seen some successes over the years and are a growing business, offering chances for progression and development across the teams. You will be coordinating a portfolio of projects, partnering with the clinical teams and sponsors.

This is a patient focused role and will see you building strong relationships with both clinical patients and cross-functional research groups in the business.

This role would suit someone with a background in clinical research, laboratory or nursing practice who are now seeking a more project-management focused role.

Responsibilities:

  • Coordinate and oversee all aspects of clinical research studies, ensuring compliance with protocols, regulations, and ethical guidelines.
  • Recruit, screen, and enrol eligible study participants, ensuring accurate documentation and informed consent.
  • Schedule and conduct study visits, procedures, and follow-up assessments according to study protocols.
  • Collect, manage, and analyse research data, maintaining accurate and complete records.
  • Liaise with study sponsors, principal investigators, and interdisciplinary teams to facilitate study implementation and resolve any issues that arise.
  • Assist in the preparation and submission of regulatory documents, including Institutional Review Board (IRB) applications and study amendments.
  • Monitor and maintain study supply inventory, ensuring availability of necessary materials and equipment.
  • Collaborate with study participants and provide education and support throughout the research process.

Qualifications:

  • Bachelor's degree in a health-related field, such as biology, nursing, or life sciences. A relevant master's degree is a plus.
  • Previous experience as a Clinical Research Coordinator or in a similar research role is preferred.
  • Strong understanding of clinical research processes, regulations, and ethical guidelines (e.g., ICH-GCP).
  • Excellent organisational skills with the ability to multitask and prioritise tasks effectively.
  • Proficiency in data collection, management, and analysis.

Joining the team as a Clinical Research Coordinator will provide an excellent opportunity to grow and become established in the area of clinical research. They have a real focus on wellness and offer extensive leadership programmes to drive a healthy workforce.

If you are interested in this opportunity, then please apply direct or contact Keeley Munday on +61 02 8310 5854 for more information.

Title: Research Coordinator

Location: Melbourne

Salary: Circa $90,000 base

Associated Keywords: Clinical trials, Research protocols, Study coordination, Participant recruitment, Informed consent, Data collection, Study monitoring, Regulatory compliance, Ethical guidelines, Institutional review board (IRB), Research documentation, Study coordination, Investigational drug/device, Study budgeting, Protocol amendments, Adverse event reporting, Data analysis, Good Clinical Practice (GCP), Study start-up, Site management

Keeley Munday Principal Candidate Consultant

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