Study Manager

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