Job Description

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Clinical Trial Assistant

Advertiser: NES Global TalentMore jobs from this company

Job Information

Job Listing Date
23 Aug 2019
Location
Sydney, North Shore & Northern Beaches
Salary
$70000 - $75000 per annum
Work Type
Full Time
Classification
Science & Technology, Other
Clinical Trial Assistant

  • Highly motivated team
  • Long term role
  • Fantastic culture
A unique opportunity has developed to join a growing CRO in Sydney.
 
The Clinical Trial Assistant (CTA) will provide logistical and administrative support to CPM and CRAs. Support the CPM in preparation of standardized clinical study tools.
 
The main responsibilities of this role include, but are not limited to the following:  
 
Maintain and manage appropriate study documentation under the direction of a CPM or CRA
Maintain tracking systems and tools to support the clinical study under the direction of CPM or CRA
Assist with clinical supply requisition and maintenance
Assist with the collection of study related documents in collaboration with the CRA
Assist with vendor management in collaboration with the CPM
Perform general administrative functions such as scheduling and organizing meetings

  • Demonstrated practical experience in co-ordinating CRO/sponsored clinical trials.
  • Working knowledge of local ethics and governance requirements for clinical research, and other statutory and regulatory requirements including comprehensive understanding of ICH GCP Guidelines.
  • Prepare investigator budget payments and tracking systems; generate tracking reports as assigned. Set up and maintain clinical investigator files and documentation.
For you to Qualify:
  • Health related undergraduate/Postgraduate degree.
  • Experience in Clinical Trials Research for at least 2 years 
  • Goal orientated to working as a CTA/SCTA for the next few years
  • Knowledge of Good Clinical Practice (GCP).
At least two years experience in clinical research and ideally in a CTA role
Bachelor’s degree or equivalent experience required (scientific or healthcare discipline preferred)
Proven organizational skills demonstrated by the ability to understand and prioritize instructions

Please get in touch for more information!

Established in 1978, NES Global Talent provides a complete range of contract and permanent talent solutions to the Oil and Gas, Power, Construction and Infrastructure, Life Sciences, Manufacturing and IT sectors worldwide. With more than 40 offices in 28 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. Offering far more than a traditional recruitment service, we fully support our contractors while they are on assignment with everything from securing visas and work permits, to providing market leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.
Christopher Parkinson
+61 2 9696 8005
christopher.parkinson@nesgt.com
Email: Please click the 'Apply Now' button below.
A unique opportunity has developed to join a growing CRO in Sydney.
 
The Clinical Trial Assistant (CTA) will provide logistical and administrative support to CPM and CRAs. Support the CPM in preparation of standardized clinical study tools.
 
The main responsibilities of this role include, but are not limited to the following:  
 
Maintain and manage appropriate study documentation under the direction of a CPM or CRA
Maintain tracking systems and tools to support the clinical study under the direction of CPM or CRA
Assist with clinical supply requisition and maintenance
Assist with the collection of study related documents in collaboration with the CRA
Assist with vendor management in collaboration with the CPM
Perform general administrative functions such as scheduling and organizing meetings

  • Demonstrated practical experience in co-ordinating CRO/sponsored clinical trials.
  • Working knowledge of local ethics and governance requirements for clinical research, and other statutory and regulatory requirements including comprehensive understanding of ICH GCP Guidelines.
  • Prepare investigator budget payments and tracking systems; generate tracking reports as assigned. Set up and maintain clinical investigator files and documentation.
For you to Qualify:
  • Health related undergraduate/Postgraduate degree.
  • Experience in Clinical Trials Research for at least 2 years 
  • Goal orientated to working as a CTA/SCTA for the next few years
  • Knowledge of Good Clinical Practice (GCP).
At least two years experience in clinical research and ideally in a CTA role
Bachelor’s degree or equivalent experience required (scientific or healthcare discipline preferred)
Proven organizational skills demonstrated by the ability to understand and prioritize instructions

Please get in touch for more information!

Established in 1978, NES Global Talent provides a complete range of contract and permanent talent solutions to the Oil and Gas, Power, Construction and Infrastructure, Life Sciences, Manufacturing and IT sectors worldwide. With more than 40 offices in 28 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. Offering far more than a traditional recruitment service, we fully support our contractors while they are on assignment with everything from securing visas and work permits, to providing market leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

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