Study manager
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Monthly Salary:
Posted:
Application Deadline:
Vacancies:
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.
Key Accountabilities:
GeneralAccountabilities
Build andmaintainengagement with Investigators other sitestaffincollaboration with other functions to ensure trial speed and effective start up conduct and close out.
Ability to manage studies and processes to agreed quality andtimelines.
Ability to proactively identify& mitigaterisks around study/site level in study execution.
Knowledge of the clinical development processunderstandconcepts and principles ofstudy design and application to manage and run studies.
Compliance with Parexel standards
Comply withrequiredtraining curriculum.
Completetimesheets accuratelyasrequired.
Submit expense reports asrequired.
UpdateCVasrequired.
Maintain a working knowledge of andcomply withParexel processes ICH-GCPs and other applicable requirements.
Previousexperience in scientific and/or regulatory medical writing.
Strong Communication Skills
Knowledge and Experience:
Keen problem-solving skills.
Fluent in both oral and written English.
Fluent in host country languagerequired.
At least 5 years in clinical practices
Education:
Minimum of BS/BA in a biomedical discipline or equivalent education/training isrequired
Required Experience:
Manager
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
