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Senior Clinical Research Associate

Job Title: Senior Clinical Research Associate
Contract Type: Permanent
Location: Sydney, Australia
Industry:
Salary: $100000 - $120000 per annum, Benefits: CAR +SUPER
Start Date: 2019-03-06
Reference: BH-103588
Contact Name: Faiza Khan
Contact Email: faiza.khan@nesgt.com
Job Published: March 06, 2019 03:00

Job Description

REIMAGINE HEAlTHCARE WITH US! ...

 

Senior Clinical Research Associate I/II Role Available  -Offers Excellent Learning Environment with Great Support & Career Development!

 

AN EXCITING OPPORTUNITY  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.Involved in Phase I-IV clinical trials with their worldwide 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 .

What is in for you:

  • Home- Based Role/Office Based flexibility-Sydney/Melbourne/Brisbane/Adelaide-
  • SCRA II-III
  • 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-IV studies, local regulatory and deep therapeutic expertise in  preferbally  Oncology.
 

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-GCP and 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.
Qualifications:

  • Must have atleast +3 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 0296968008 you can share your resume to faiza. khan @ nesgt. com