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2 weeks ago
**Project Manager / Lead Coordinator, ACTRIS**
**Overview**
The Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together six national R&D, clinical translation and service programmes to advance clinical research and innovation for Singapore, and establish important capabilities for a future-ready healthcare system.
The Business Entities under CRIS include:
- Singapore Clinical Research Institute (SCRI)
- National Health Innovation Centre (NHIC)
- Advanced Cell Therapy and Research Institute, Singapore (ACTRIS)
- Precision Health Research, Singapore (PRECISE)
- Singapore Translational Cancer Consortium (STCC)
- Cardiovascular Disease National Collaborative Enterprise (CADENCE)
Together, CRIS makes a positive difference to Singapore patients and researchers by ensuring that these clinical research platforms and programmes are at the cutting edge of capability development and innovation. If you are as passionate as we are in clinical trials and research, we want you
**ACTRIS**
The Advanced Cell Therapy and Research Institute, Singapore (ACTRIS) was established to meet the increasing clinical demand of using cellular therapeutics to treat various life-threatening diseases. ACTRIS’ vision is to be the national and regional Centre of Excellence for discovery, process development and manufacturing of cellular-based therapeutics across the broad spectrum of immunotherapy and regenerative medicine, encompassing both investigational and approval products for the local market. We also provide value-added services such as workforce training, regulatory facilitation and ancillary material standardization, pertaining to delivery of cellular therapy to patients.
**What you will be working on**
- Oversee and is accountable for overall planning, execution and delivery of projects at ACTRIS, including project timelines, key milestones, budget, scope and risks.
- Co-ordinate internal efforts to ensure all aspects of incoming and ongoing projects are current with relation to set requirements and are aligned with organizational strategies.
- Act as an interface and communicate progress to internal and external (after project moves to clinical manufacturing) stakeholders with respect to the project concerned.
- Collaborate with cross-functional teams to track and provide project status updates to senior management and other key stakeholders, including supporting the development of relevant presentation.
- Maintain oversight of outstanding project-related documents for incoming and ongoing projects.
- Ensure timely delivery of all required QMS deliverables and activities.
- Serve as the biosafety and workplace safety expert for the organization.
- Any other scope assigned by reporting officer (such as but not limited to, e.g. training).
**What we are looking for**
- Degree in Life Sciences/Medical Sciences or equivalent.
- 5 years of relevant project management experience in a fast-paced environment (e.g. planning, risk management, status reporting, budget tracking, stakeholder management and resource planning), in particular with understanding and running of cell, tissue and gene therapy products (CTGTP) Good Manufacturing Practice (GMP) projects.
- Team player with ability to forge strong working relationships with cross functional teams / multiple stakeholders.
- Excellent written and verbal communication skills.
- Strong negotiation and problem-solving skills.
- Results orientated, flexible and able to handle changing priorities.
- Certifications (PMP, Lean, Scrum, biosafety) and knowledge of Quality Systems & relevant regulatory regulations will be advantageous.
- Prior experience in clinical and biomedical research laboratory with supervisory role is an added advantage.
**What you need to know
