Study manager (FSP)

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

• Comply with required training curriculum.

• Complete timesheets accurately as required.

• Submit expense reports as required.

• Update CV as required.

• Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable requirements.

• 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