Covance

Clinical Research Assoc. I MEA

Job Location(s) AU-Adelaide
Job Number
2021-60814
Job Category
Clinical Research Associates
Position Type
Full-Time
Telecommute
No

Job Overview

ADVANCE YOUR CAREER WITH THE MONITORING EXCELLENCE ACADEMY
 
In the MEA CRA role you will receive the support and guidance of a mentor. Many graduates continue to stay in touch with their mentors beyond the program.
 
WORKING WITH EXCEPTIONAL PEOPLE ON EXTRAORDINARY PATHS
 
Covance CRAs thrive in an encouraging team environment as they help shape the future of clinical research. Our MEA program is just one example of how Covance works with you to build your career in a supportive setting.
 
A CLEAR PATH TO BECOME AN OFFICE OR HOME-BASED CLINICAL TEAM MEMBER
 
Your MEA training will kick off with virtual and/or face-to-face training, either in the office or from your own home. If you are hired into a home-based position, you will participate in a live in-person training with other MEA participants. You’ll then get ready to travel for observational and co-monitoring visits. Here, you’ll learn best practices and start site visits with the goal of becoming an independent CRA.
 
AN OPPORTUNITY TO ADVANCE YOUR CAREER THROUGH A COMBINATION OF HOME-BASED TRAINING AND TRAVELLING.
 
Apply now for our current opening in Adelaide, Australia.

Education/Qualifications

Minimum Required:
 
♦External Candidates o University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)

 
 

Experience

o A minimum of 2 years of experience in a related role (e.g. site management, in-house CRA, study coordinator, research nurse, etc.)
♦ Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements
♦ Basic understanding of the clinical trial process
♦ Valid Driver’s License
Preferred:
♦Working knowledge of Covance SOPs for site monitoring
 
♦ Ability to monitor study sites according to protocol monitoring guidelines, SOPs, ICH Guidelines and GCP
♦ Ability to work within a project team
♦ Good planning, organization and problem solving abilities
♦ Good communication skills, oral and written
♦ Good computer skills
♦ Works efficiently and effectively in a matrix environment
♦ Fluent in local office language and in English, both written and verbal
 
Preferred:
♦One (1) or more additional years of experience in a related field (i.e., medical, clinical, pharmaceutical laboratory, research, data analysis, data management or technical writing) is preferred.

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