Research Scientific Coordinator (Kota Kinabalu)

Primary Responsibilities:

• Lead relevant project data analyses, manuscript preparation and/or contribution to other relevant manuscripts, and dissemination of research findings/outputs.
• Develops accurate source materials and ensures compliance from site staff.
• Maintain quality assurance and supervision if relevant research laboratories and train staff in the use of serological and other laboratory techniques associated with the projects.
• Ensure data is collected and stored appropriately and in accordance with ethical and cultural guidelines.
• Develop and maintain productive, cooperative working relationships with other members of the research team, as well as external collaborators.
• Occasional travel to attend sponsor study training meetings (as required).

SELECTION CRITERIA

Essential:

• Bachelor (or Master’s level) science degree.
• Specific laboratory skills related to the conduct and analysis of multiplex microsphere immunoassays and molecular pathogen detection methods.
• Demonstrated experience of staff training in the use of serological and molecular laboratory techniques.
• Experience and competence in the use of a range of information technologies and applications such as R statistical software and electronic data collection software.
• Initiative, good judgement and strong problem-solving skills with demonstrated ability to work under broad direction independently or as part of a multidisciplinary team.
• Proven organizational skills, strong record keeping abilities and experience in managing resources to meet objectives and deadlines.
• Demonstrated ability to think analytically and critically and to synthesize relevant data in the stated area(s) of interest.
• Highly developed written and oral communication skills, ability to interact effectively with a range of stakeholders across geographical locations.
• An understanding of research ethics, including confidentiality, privacy and anonymity and how to maintain while working in the research setting and willingness to learn and adhere to relevant guidelines (Good Clinical Practice Guidelines).
• Knowledge of GCP, federal, state, and local regulations, including HIPAA policies and procedures.