Senior Asst/Project Manager, Clinical Trials & Research Unit (1-yr contract)

Changi General Hospital; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A healthcare institution in Singapore seeks a Senior Assistant/Project Manager for its Clinical Trials & Research Unit. The role involves leading project discussions, managing compliance with regulations, and assisting in project organization. Candidates should have a degree in Life Sciences or related fields, at least 4 years of relevant experience in clinical project management, and strong interpersonal skills. This is a 1-year contract position.

Qualifications

• At least 4 years relevant experience in clinical project management.
• Advanced proficiency in Project Management and trial procedures is an advantage.

Responsibilities

• Lead project discussions independently.
• Ensure compliance with applicable regulations.
• Assist Principal Investigators in project organization.
• Draft project progress reports and manuscripts.

Skills

Team Player

Time Management

Interpersonal Skills

Multi-tasking

Self-motivated

Education

Degree in Life Sciences/Pharmaceutical Science/Clinical Trials Management

Job description

Senior Asst/Project Manager, Clinical Trials & Research Unit (1-yr contract)

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
• 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
• 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
• Assist in drafting relevant project progress reports including analysis, interpretation and reporting process of findings and results, as well as assist in preparation of manuscripts, reports and presentation materials (if applicable)
• Assist in review and implementation of department SOPs and work instructions
• Take on projects as assigned from time to time

Qualifications

• 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

Only shortlisted candidates will be notified.