Job Description

• 5 Days [ 8:30am -6:00pm] * Near Kent Ridge and Queenstown * Biotechnology / Pharmaceutical / Consumer Healthcare * Life Science / Pharmacy / Technical / Clinical Interested applicants can send your resume to WhatsApp: +65 90814261 and 5 Days [ 8:30am -6:00pm] Near Kent Ridge and Queenstown Biotechnology / Pharmaceutical / Consumer Healthcare Life Science / Pharmacy / Technical / Clinical Interested applicants can send your resume to WhatsApp: +65 90814261 and allow our Consultants to match you with our clients. No Charges will be incurred by Candidates for any service rendered. Requirements: Diploma, Bachelor's or Master's degree in Life Sciences/Biomedical Science, or equivalent combination of education and experience More than 2 years technical/clinical study management or managerial experience in project management Responsibilities: Manages projects from proposal development to final deliverables. Based out of Singapore, managing projects in South-East Asia across various phases and functional areas. The projects would initially be focussed on initiating validation studies for Onco-PDO Phenotype- Driven Precision Oncology technology from Patient Derived Tumours. Project Administration: Acts as primary liaison to ensure project / clinical study organization, launch, conduct / implementation, management and closeout. Financial Aspects: Review budgets, expenses and project financial status. Establish and manage contracts with vendors. Project Planning: Develops and maintains project plans in accordance with Standard Operating Procedures (SOPs) and Work Instructions (WI). Project Tracking: Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools. Produces and distributes status, resourcing, and tracking reports to appropriate team members and senior management. Alerts senior management to potential issues and ensures necessary corrective and preventive actions are taken. Regulatory Affairs: Ensure project documentation are complete and audit ready. Oversee regulatory documents collection and submission process. Participate in internal and external audits/inspections. May represent company at professional meetings or seminars. Performs other work-related duties as assigned.