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.
Key Accountabilities:
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.
Skills:
- Previous experience 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 language required.
- At least 5 years in clinical practices.
Education:
- Minimum of BS/BA in a biomedical discipline or equivalent education/training is required.