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Senior Clinical Trials Manager

RandstadHong Kong

30+ days ago

Job description

job details

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

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.

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%)

humanforward

skills

no additional skills required

qualifications

no additional qualifications required

education

Bachelor Degree

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