Senior Research Fellow

Reporting directly to Principal Investigator, you will be involved in various international and local clinical research projects. You will assist in project planning, and ensure that pre-established work scope, study protocol, and regulatory requirements are followed. You will serve as principal administrative liaison for the projects. Recruiting and coordinating research subjects, as appropriate, are among the responsibilities.

You will be responsible for the following:

• Compliance with the ICH GCP, HBRA, HSA, IRB, and other applicable regulatory and ethical requirements as well as hospital policies
• Monitor the progress of research activities
• Develop and maintain records of research activities, and prepare periodic and ad hoc reports, as required by investigators, administrators, funding agencies, and/or regulatory bodies
• Assist in drafting DSRB ethics application, HSA clinical trial authorization application, amendments, and status reports
• Assist investigators in screening, determining eligibility, recruitment, and follow-up visits of enrolled subjects
• Assist investigators in obtaining informed consent and documenting of informed consent process
• Ensure safety and well-being of subject
• Assist investigators in safety reporting to DSRB and HSA within stipulated timelines
• Act as the primary liaison between all Singapore sites and the global trial management teams
• Communicate with site study team members regarding any trial updates (protocol amendments, safety reports)
• Maintain Investigator Site File and ensure that all documents are complete and up to date
• Ensures the smooth and efficient day-to-day operation of research and data collection activities
• Handle biological samples and keep track of sample transfer
• Coordinates the day-to-day activities of any technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives
• Assist PI in writing grant, procurement process, as well as budgeting
• Train research coordinators for the trials
• Occasional night and weekend work when necessary
• Other tasks when needed

Qualification Required and Area of Discipline

• Candidate should hold minimum of BSc in Life Science or an equivalence qualification

Required Competencies and Capabilities (Skills, Experiences and Professional Licences)

• Minimum 5 years working in clinical/life sciences research
• Competency in ethics applications as well as communication with IRB
• Familiarity with inpatient ward setting, working environment as well as medical equipment
• Experience in studies related to invasive mechanical ventilation, dialysis and ECLS is preferred but not essential
• Familiarity with certain laboratory procedures including sample processing, analysing data using various scientific techniques (flow cytometry, immunofluorescence, proteomics)
• Demonstrated understanding of scientific techniques and ethical considerations in clinical protocols
• Competence in analysing feasibility of protocol procedure, implementing the procedures, and planning appropriate workflow for team members
• Ability to work in an interdisciplinary environment
• Experience in safety management
• Experience in training junior staff and students
• Good organization skills and administrative meticulousness
• Ability to multi-task, work independently, problem solve, as well as work as part of a team
• Excellent communication