Clinical Trials
7 days ago
You will be part of the operational team in Clinical Trials & Research Unit (CTRU). You will work alongside members of the project team to provide project management service for projects that fulfil eligibility criteria under oversight of the Project Manager.
Responsibilities:
- Able to lead or facilitate project discussions independently, effectively and efficiently
- Ensure smooth and effective conduct of research projects according to applicable regulations by informed study teams
To assist Principal Investigators in project organization which includes the following:
Budget estimate and planning
- Grant(s) application (if applicable)
- Submission to ethics and regulatory bodies, and tracking the approval status
- Sourcing for external vendors/suppliers and assisting in negotiation of acceptable costs
- To manage, guide, supervise and review the performance evaluation of the project team members and review the quality of the work completed by the project team on a regular basis
- To assist in the drafting of relevant project progress reports including the analysis, interpretation and reporting process of findings and results as well as to assist in the preparation of manuscripts, reports and presentation materials (if applicable)
- Assist in the review and implementation of department SOPs and work instructions
- To take on projects as assigned from time to time
Requirements:
- Degree in Life Sciences/ Pharmaceutical Science/ Clinical Trials Management
- At least 4 years relevant experience in clinical project management. Those with advance proficiency in Project Management and expert knowledge of trial procedures, institutional, CIRB & regulatory authority requirements for managing clinical trial would be at an advantage
- Team Player and ability to multi-task, with good time management
- Self-motivated and ability to work in a fast-paced environment
- Good interpersonal relationship skills
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