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Clinical Research Associate II/III

Job Title: Clinical Research Associate II/III
Contract Type: Permanent
Location: Melbourne C B D, Australia
Industry:
Salary: $110000 - $120000 per annum, Benefits: car+super
Start Date: 2019-01-17
Reference: BH-97142-2
Contact Name: Faiza Khan
Contact Email: faiza.khan@nesgt.com
Job Published: January 17, 2019 23:52

Job Description


Clinical Research Associates II/III.

A CRA level II/III is required by a global CRO for a home based/office based position nationwide.

  • You may also be office based/home based, if you’d prefer at the office in Melbourne only.
  • Permanent-Full Time Position.
  • The role involves independent monitoring Clinical Trials in various therapy areas, mainly in Oncology Phase I- IV clinical study sites in Australia.
You will join like-minded collaborative professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing top CRO firm, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world.

Role/Description:

  • Responsible for Site management, set up, routine monitoring and close out visits, feasibility reports.
  • To perform the activities associated with the site-level feasibility, evaluation, initiation, patient recruitment and retention, monitoring and collection of data, and closeout of clinical trial sites in the geographic area assigned.
  • Writing monitoring reports.
  • Liaising with investigators and other members of a multi-disciplinary team.
  • Variety of therapy areas, which may include oncology, cardiovascular, CNS, respiratory and/or infectious diseases.
  • Delivering onsite training of investigators and staff.
  • Monitoring trial progress and ensuring that the project timelines are met.
Qualifications:

  • University degree in Life Sciences, Pharmacy, MD or RN or an equivalent combination of education, training and experience.
  • Local Experience: independent monitoring atlest  1.5-3 years , with full scope of monitoring responsibilities within Phase I/II/III Clinical Trials.
  • Independent monitoring experience in Australia.
  • Experience in regulatory submissions, contract negotiations, site management and feasibility assessment.
  • Preferably with Experience in Oncology, Infectious Disease or Neurology.
  • Full working rights in Australia.
We provide high-quality employment, competitive salary, excellent working conditions and a personable supportive environment. It is a great chance to join the company that really cares for its people, and invests in their professional development and success.

Please feel free to contact at faiza.khan @ nesgt. com for more information/Call 02-9696 8008.