Parexel
From Parexel's careers page
Status: listed on the employer's own careers page when we last checked (daily). Confirm on their site before applying.
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's 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 we're committed to making a difference.
General Accountabilities
Build and maintain engagement with Investigators, other site staff in collaboration with other functions, to ensure trial speed and effective start up, conduct and close out.
Ability to manage studies and processes to agreed quality and timelines.
Ability to proactively identify & mitigate risks around study/site level in study execution.
Knowledge of the clinical development process, understand concepts and principles of study design, and application to manage and run studies.
Compliance with Parexel standards
Complies with required training curriculum.
Completes timesheets accurately as required.
Submits expense reports as required.
Updates CV as required .
Maintains a working knowledge of and complies with Parexel processes, ICH- GCPs and other applicable requirements.
Previous experience in scientific and/or regulatory medical writing.
Strong Communication Skills.
Keen problem-solving skills.
Fluent in both oral and written English.
Fluent in host country language required.
At least 5 years in clinical practices.
Minimum of BS/BA in a biomedical discipline or equivalent education/training is required.
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