<p>Create clinical development strategy; establish good relationship with KOLs
Select the most suitable CROs and vendors for the studies and oversee their tasks
Senior Manager will develop regulatory strategy and documents including CSR, CTD and M3 for J-NDA and respond to inquiries from external authorities. You will also direct development of SOPs within department.
The ideal candidate must have at least 10 years of working experience in clinical development and/or project management leading 3-5 trials and experience of managing CROs. Candidates with liver disease or oncology area background with KOL connections are strongly recommended to apply.
Please contact Tserendolgor Sanduijav
For more information at
|応募資格||clinical operations, submission documents, SOPs and managing CROs|
|事業内容||This globally successful pharmaceutical company is on the track to focus more on oncology and immuno-oncology and launch competitive products.|