Clinical Trial Manager 2 (FSP)
Clinical Trial Manager 2 (FSP)
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Job Description
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds 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 were 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:
Bachelors degree
Major focus: Biomedical Life Sciences
Required Experience:
Manager
Employment Type
Full-Time
