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.
Responsibilities
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.
Requirements
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 Skills: Previous experience in scientific and/or regulatory medical writing.
Keen problem-solving skills.
Fluent in both oral and written English.
Fluent in host country language required.
At least 5 years in clinical practices Education: Minimum of BS/BA in a biomedical discipline or equivalent education/training is required
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