- SalaryCompetitive salary
- LocationEast Ryde
- Job type Full Time
- DisciplineClinical Research
- ReferenceBH-41696
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Clinical Project Manager
Job description
Benefits
About the company
Join a global pharmaceutical leader known for innovative drug development and a strong presence in the Asia Pacific region. This company specializes in various therapeutic areas and is renowned for its commitment to improving health outcomes worldwide, offering a collaborative and dynamic work environment.
About the opportunity
As a Clinical Trial Manager, you will manage local-level trial activities for trials in the Asia Pacific region. Reporting to the Clinical Research Manager, you will lead studies following ICH-GCP guidelines, corporate SOPs, and regulatory requirements. This role is crucial for driving trial feasibility, execution, and overall therapeutic area development strategies. You'll work closely with internal and external stakeholders, ensuring the success of the clinical trials.
Duties
Skills and Experience
Culture
Join a supportive, innovative, and collaborative team dedicated to improving health outcomes globally.
How to Apply
Click apply or contact Davina Ocansey-Gibson, Senior Recruitment Consultant on +61 2 8877 8712 for a confidential discussion.
- Lead innovative drug development projects
- Opportunities for career growth and professional development
- Supportive work-life balance with flexible working arrangements
About the company
Join a global pharmaceutical leader known for innovative drug development and a strong presence in the Asia Pacific region. This company specializes in various therapeutic areas and is renowned for its commitment to improving health outcomes worldwide, offering a collaborative and dynamic work environment.
About the opportunity
As a Clinical Trial Manager, you will manage local-level trial activities for trials in the Asia Pacific region. Reporting to the Clinical Research Manager, you will lead studies following ICH-GCP guidelines, corporate SOPs, and regulatory requirements. This role is crucial for driving trial feasibility, execution, and overall therapeutic area development strategies. You'll work closely with internal and external stakeholders, ensuring the success of the clinical trials.
Duties
- Lead drug development plan input projects and conduct trial feasibility and site selection
- Oversee trial start-up activities, including budget negotiation and forecasting
- Coordinate ethics and regulatory submissions
- Facilitate recruitment activities and liaise with vendors
- Ensure CRAs are trained and monitoring trials according to requirements
- Maintain Corporate Clinical Trial Management System and oversee TMF activities
- Participate in global teleconferences and local team meetings
- Prepare for and participate in trial audits and inspections
- Execute trial close-out activities successfully
Skills and Experience
- Min 2 years of Clinical PM experience within a sponsor or CRO environment
- Tertiary qualifications in biological, health, or medical sciences, pharmacy, nursing, or medicine
- Postgraduate qualifications highly regarded
- Research and project management experience with functional knowledge of local regulations
- Experience leading a clinical project team
Culture
Join a supportive, innovative, and collaborative team dedicated to improving health outcomes globally.
How to Apply
Click apply or contact Davina Ocansey-Gibson, Senior Recruitment Consultant on +61 2 8877 8712 for a confidential discussion.