Clinical Trial Assistant
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Job Location:
Monthly Salary:
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
The Clinical Trial Administrator (CTA) is responsible for performing a variety of research database and clerical duties of a complex and technical nature in support of multiple clinical trials. This position also provides administrative support to clinical teams by reviewing vendor invoices for accuracy against budget tracking vendor payments in compliance with federal regulations and taking meeting minutes during project team meetings.
Bachelors degree in a related field or equivalent combination of training education and work experience preferred
Three (3) or more years of experience in a clinical administrative or regulatory role in a pharmaceutical or CRO environment
Knowledge of FDA GCP-ICH Guidelines and local regulatory requirements
Knowing the objectives of the various stages of clinical development
Ability to demonstrate a high level of competency relating to administrative and clerical responsibilities procedures and systems
Excellent verbal and written communication interpersonal organizational and time management
Required Experience:
Junior IC
Key Skills
- CSS
- Cloud Computing
- Health Education
- Actuary
- Building Electrician
About Company
Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our the ... View more
