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