Our client, a global pharmaceutical organisation, is looking for a Senior Study Manager to join them in the delivery of Phase I-IIIb studies standards relating to the Asia Pacific Region.
Based in Singapore and reporting to the Clinical Operations Manager, you will lead and manage a high performing drug development team to ensure the success of our client's research and development within a culturally diverse region.
You will be responsible for the successful execution of clinical studies, the writing of study protocols, and in ensuring compliance with all regulatory and the use of good clinical practice during the conduct of assigned studies, including oversight of the study teams and CROs/other vendors.
You will be a part of a global study group that will collaborate with other team members including Clinical Research, Clinical Pharmacology, Statistics, Data Management, Regulatory Affairs, Project Management and Clinical Supplies to develop a study timeline and budget.
This development centre is testament of our client's commitment to develop an optimal structure for its global clinical development operations. The Senior Study Manager will be an integral member of this team.
Educated to a minimum of a first science degree, you will demonstrate an excellent clinical research background with at least 5 years of clinical trial management experience including a minimum of one year of monitoring experience. You must have multiple-site experience in the Asian region specifically SEA. Additional experience in India and China is desirable.
How to apply for the Senior Study Manager role:
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Send your completed job application through to us for processing.
Alternatively, for a confidential discussion concerning the Senior Study Manager opportunity you can telephone Laura Thomas on +65 6533 5708. Please be sure to quote 10406 in all correspondence relating to this role.
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