Job Title: Experienced Clinical Research Associate FSP
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About the Role
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This is an exciting opportunity to join our team as a Senior Clinical Research Associate, where you will be responsible for conducting site feasibility and identification, initiation, monitoring visits, and close-out activities.
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As a member of our global clinical research organisation, you will work on a wide range of trials, including early Phase Oncology trials. You will have the opportunity to develop your skills and expertise in trial management, working closely with our client's study team and collaborating with colleagues across different regions.
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Our ideal candidate will possess excellent communication skills, strong analytical skills, and the ability to work independently with minimal supervision. You will also have a degree in Pharmacy or a related field, and at least 2+ years' experience in on-site monitoring, preferably with global trials and early Phase Oncology trial monitoring.
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Responsibilities
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* Perform all aspects of CRA duties from site feasibility and selection through to close-out visits and database lock
* Lead site identification and initiation activities
* Oversee all aspects of study site management to ensure high-quality data
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Requirements
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* Degree in Pharmacy or a related field
* At least 2+ years' experience in on-site monitoring with global trials and early Phase Oncology trial monitoring
* Excellent communication skills
* Ability to work independently with minimal supervision
* Flexibility to travel for monitoring visits as required
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What We Offer
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We offer a competitive salary and a range of benefits, including annual leave entitlements, health insurance, retirement planning, and life assurance.
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In addition, we provide opportunities for professional development and growth, and a collaborative and inclusive work environment that supports diversity and inclusion.
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