Project Manager, ACTRIS (GMP experience mandatory)

Consortium For Clinical Research And Innovation Singapore; Outram; On-site; CAD 80,000 - 100,000; Full time

Job summary

A clinical research organization in Outram is looking for a Project Manager with at least 5 years of project management experience in GMP environments. The role involves overseeing project planning and execution, maintaining communication with stakeholders, and ensuring compliance with regulatory standards. Ideal candidates will have a degree in Life Sciences and excellent communication skills. A 3-year contract will be offered, renewable.

Qualifications

• 5 years of relevant project management experience in a fast-paced environment.
• Understanding and running of cell, tissue and gene therapy products (CTGTP) GMP projects.
• Prior experience in clinical and biomedical research laboratory with supervisory role is an added advantage.

Responsibilities

• Oversee and is accountable for overall planning and execution of projects.
• Communicate progress to internal and external stakeholders.
• Maintain oversight of outstanding project-related documents.

Skills

Project management

Communication skills

Problem-solving

Team player

Education

Degree in Life Sciences/Medical Sciences or equivalent

Tools

Project Management Professional (PMP)

Lean

Scrum

Job description

Project Manager, ACTRIS (GMP experience mandatory)

Consortium For Clinical Research And Innovation Singapore – Outram

The Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together seven 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.

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.

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 stakeholders with respect to the project concerned.
• Apply analysis to understand, forecast and communicate schedule trends and status of resources such as clean rooms, supplies, equipment etc.
• 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, 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

Successful candidate will be offered a 3-year contract, renewable. We regret that only shortlisted candidates will be contacted.

CRIS is an equal opportunities employer and welcomes applications from qualified candidates.