Our client, a world-class leading pharmaceutical manufacturing company, is currently looking for a Clinical Trials Manager (Oncology) to join their expanding team.
about the job. ...
Manages geographical regions of large complex clinical trials and independently manages all components of a small less complex study (including phase 1 studies), per business needs
Collaborates with other functions (and vendors) on how to best achieve their study goals and objectives and communicates cross-functionally to ensure project team goals are met, in partnership with global study team
Provides oversight of study sites/region and reviews routine regulatory documents to ensure that CROs are in compliance with protocols, regulatory requirements, SOPs, and monitoring plans
skills & experiences required.
For Clinical Trials Manager, the candidate must have a minimum of 5 years of experience and a BS or BA in a relevant scientific discipline. For candidate having 7+ years of relevant experience, Senior Clinical Trials Manager may be offered
Ideally have 2+ year regional oncology study management experience in Asia Pacific region and 5+ years site monitoring experience in Hong Kong and/or Asia Pacific region
Thorough knowledge of Regulatory Regulations, ICH Guidelines, and GCP governing the conduct of clinical studies
International and regional travel is required (approximately 20%)
Interested individuals can click apply now and send through an updated resume in WORD format. For a more comprehensive list of current opportunities, please visit https://www.randstad.com/jobs/q-hong-kong/ or contact Jessica Cheung at + 852 6285 6991 or email jessica.cheung@randstad.com.hk
#humanforward
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about the company.
Our client, a world-class leading pharmaceutical manufacturing company, is currently looking for a Clinical Trials Manager (Oncology) to join their expanding team.
about the job.
Manages geographical regions of large complex clinical trials and independently manages all components of a small less complex study (including phase 1 studies), per business needs
Collaborates with other functions (and vendors) on how to best achieve their study goals and objectives and communicates cross-functionally to ensure project team goals are met, in partnership with global study team
Provides oversight of study sites/region and reviews routine regulatory documents to ensure that CROs are in compliance with protocols, regulatory requirements, SOPs, and monitoring plans
skills & experiences required.
For Clinical Trials Manager, the candidate must have a minimum of 5 years of experience and a BS or BA in a relevant scientific discipline. For candidate having 7+ years of relevant experience, Senior Clinical Trials Manager may be offered
...
Ideally have 2+ year regional oncology study management experience in Asia Pacific region and 5+ years site monitoring experience in Hong Kong and/or Asia Pacific region
Thorough knowledge of Regulatory Regulations, ICH Guidelines, and GCP governing the conduct of clinical studies
International and regional travel is required (approximately 20%)
Interested individuals can click apply now and send through an updated resume in WORD format. For a more comprehensive list of current opportunities, please visit https://www.randstad.com/jobs/q-hong-kong/ or contact Jessica Cheung at + 852 6285 6991 or email jessica.cheung@randstad.com.hk
#humanforward
show more
skills
no additional skills required
qualifications
no additional qualifications required
education
Bachelor Degree
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