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
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