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Job details

Location
Melbourne
Salary
120,000 - 125,000 + 21,000 + Car Allowance + Super + Bonus
Job Type
Contract
Ref
BH-40355
Contact
Maddy Rhodes-Laird
Contact email
Email Maddy
Contact phone
+613 9938 7101
Posted
9 months ago

Job details

Location
Melbourne
Salary
120,000 - 125,000 + 21,000 + Car Allowance + Super + Bonus
Job Type
Contract
Ref
BH-40355
Contact
Maddy Rhodes-Laird
Contact email
Email Maddy
Contact phone
+613 9938 7101
Posted
9 months ago
About

Our client is a worldwide science-led biopharmaceutical company, they are involved in the research, development, manufacture, and supply of medications that seek to make a substantial difference to the lives of Australians. They work across a few main therapy areas which are Oncology; Respiratory, Inflammation and Autoimmunity (RIA); Cardiovascular and Metabolic Diseases (CVMD).

Benefits:
  • Work for a sponsor
  • Be a part of a global team!
  • Large car allowance
  • Exposure to Cardiology & Biopharma
About the role:
As a SCRA you will have local responsibility for the delivery of the studies at allocated sites and are an active participant in the local study team(s). The SCRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a suitable and effective manner. The SCRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study.
The SCRA is accountable for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.

About you:
  • Bachelor degree in related discipline, preferably in life science, or equivalent qualification
  • Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP. Good knowledge of relevant local regulations.
  • Good medical knowledge and ability to learn relevant AZ Therapeutic Areas. Basic understanding of the drug development process.
  • Solid understanding of Clinical Study Management including monitoring, study drug handling and data management.
  • Excellent attention to details.
  • Good written and verbal communication skills.
  • Proficient collaboration and interpersonal skills.
  • Great negotiation skills.
  • Ability to travel nationally/internationally as required.

How to Apply

Click apply or contact Maddy Rhodes–Laird, Senior Recruitment Consultant on 03 9938 7101 for a confidential discussion.

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