Consortium for Clinical Research and Innovation Singapore | Lead Project Coordinator
1 day ago
Lead Project Coordinator / Manager, Translational Services & Regulatory Management, 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)
Advanced Cell Therapy and Research Institute, Singapore (ACTRIS)
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
Co-ordinate internal efforts to ensure program documents, reports, tools and metrics are current with relation to set program cadence/ client requirements.
Communicate progress to internal and external stakeholders with respect to the project concerned.
Assist Dept Head in overseeing the operations of the translational labs including equipment, IT and other relevant matters.
Utilize ACTRIS’ technical capabilities and service offerings to direct customers towards maximizing the use of ACTRIS’ services and resources.
Apply analysis to understand, forecast and communicate cost/ schedule trends, performance analysis, and status.
Collaborate with cross-functional teams to support the development of board/ management updates and presentations with a focus on the specific projects including scheduling.
Maintain project business data/ reports with Finance, other departments and external clients.
Identify / resolve business and technical issues affecting the project.
Serve as the biosafety coordinator for the organization.
Maintain knowledge of cellular-based immunotherapy and regenerative medicine.
Any other scope assigned by reporting officer.
What we are looking for
Degree in Business Administration, Communications, Life Sciences/Medical Sciences or equivalent. Advanced degree (such as PhD) in life sciences or related fields will be an advantage.
5 years of relevant experience in fast pace environment.
Ability to forge strong working relationships at all levels/ stakeholders.
Excellent written and verbal communication skills.
Results orientated, flexible and able to handle changing priorities.
Certifications (PMP, Lean, Scrum, biosafety) will be advantageous.
Prior experience in clinical and biomedical research laboratory with supervisory role is an added advantage.
What you need to know
Successful candidate will be offered a 3-year contract, renewable. We regret that only shortlisted candidates will be contacted.
For more information about CRIS and the Business Entities, visit our websites below:
CRIS –
SCRI –
NHIC –
ACTRIS –
PRECISE –
STCC –
CADENCE –
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