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- Working independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation
- Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
- Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
- Managing sponsor generated queries efficiently and responsible for study cost effectiveness
- Dependent on level of experience you may assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects
- 18 months+ of monitoring experience in phase I-III trials as a CRA
- Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
- Native local language and conversational English is a must
- Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner
- Ability to produce accurate work to tight deadlines within a pressurized environment
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IndustryContent type
BlogsPublish date
04/10/2024
Summary
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Who we are
Salary
Location
Melbourne
Department
Clinical Monitoring
Location
Melbourne
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
CRA II / Senior CRALocation: Melbourne, Sydney, Perth As a Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthca
Reference
2024-109410
Expiry date
01/01/0001
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Salary
Location
Argentina
Department
Clinical Monitoring
Location
Argentina
Remote Working
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Description
As Clinical Research Associate (CRA), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. A CRA is a professional who cont
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2023-103904
Expiry date
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Salary
Location
Argentina
Department
Clinical Trial Management
Location
Argentina
Remote Working
Remote
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions.
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2023-103323
Expiry date
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Salary
Location
Belgium, United Kingdom, Denmark, France, Spain, Germany, Netherlands, Switzerland
Department
Medical Affiars & Medical Writing Roles
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Belgium
Denmark
France
Germany
Netherlands
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Switzerland
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Salary
Location
Boston
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Boston
Remote Working
Office Based
Job Categories
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Reference
2023-107609
Expiry date
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