Clinical Trial Manager 2 (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 and Patient Organizations (POs), in collaboration with other functions, to ensure trial speed and effective start up, conduct and close out.
• Establish and maintain relationships with external experts, investigational sites, Patient Organizations and other stakeholders by coordinating and ensuring cross-functional collaboration amongst CD&O and appropriate functions (i.e Medical Affairs, Market Access, PAR) on regional/ local level.
• Supports CTL to ensure issues are raised to Evidence team for timely action or mitigation.

Compliance with Parexel Standards:

• Complies with required training curriculum
• Completes timesheets accurately and timely 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:

• Minimum 1-2 year experience of project management experience

• Strong Communication Skills

Knowledge and Experience:

• Ability to build and maintain strong relationships of mutual value
• Fluent in both oral and written English
• Fluent in host country language required

Education:

• Bachelor’s degree

• Major focus: Biomedical Life Sciences

Originally posted on Himalayas