Job Title: SCRA/CRA
Contract Type: Permanent
Location: Sydney, Australia
Salary: $105000 - $110000 per annum, Benefits: Plus Car and Super
Start Date: 2019-03-06
Reference: BH-97458-2
Contact Name: Faiza Khan
Contact Email:
Job Published: March 06, 2019 00:59

Job Description

Senior Clinical Research Associate I-II(SCRA)-REIMAGINE HEAlTHCARE WITH US! ...


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

Offers Excellent Learning Environment with Great Support & Career Deveopment across nation and internationally.
AN EXCITING OOPORTUNITY  with an award winning Leading CRO with 800+Clinical trials, 140+Sponsors, 22,000+Patients.This Multinational CRO is being recognised industry-wide for their dedication to the future of clinical development.Involed in Phase I-IV clinical trials with their worlwide reach and major focus exclusively in Asia Pacific region.
The award of new projects has resulted in multiple opportunities arising for well-experienced  Clinical Research Associates to join and support  their team in  Sydney/Melbourne/Brisbane/Adelaide  - Australia wide .

Whats in for you

  • SCRA II Home- Based Role/Office Based flexibility-Sydney/Melbourne/Brisbane/Adelaide-
  • Travel(Locally and interstate sites)-50%
  • MultiSponsor -exposure
  • Attractive remuneration Package with Car allowance and Super.
  • Shared Bonus Scheme-2-7%depending on the performance
  • Offer excellent career goals and personal growth along with personal benefits
  • The client focus on clinical trial Phase I-IVstudies, local regulatory and deep therapeutic expertise in  preferbally  
The Role Responsibilities:
  • Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out. 
  • Prepare, organise, conduct and follow-up routine monitoring and close out visits as per relevant study plan
  • Ensure ethics submissions are made by investigator sites in a timely manner.
  • Adherence to ICH-GCPand any other regulatory guidelines and requirements including adverse events and serious adverse event reporting
  • Compliance with mandatory SOPs as agreed for the study
  • Being a resource for other CRAs, mentoring junior-level staff and sharing knowledge and best practices.
  • Participating in training offered to increase therapeutic knowledge and keeping current with regulations and TGA guidance.
  • Must have atleast +4 years of Experience in the similar capacity.
  • Including conducting independent monitoring visits, from either a pharmaceutical company or a CRO environment.

 Please get in touch for a confidential chat at 02-96968008 you can share your resume to 
faiza. khan


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