Key Responsibility Areas

• The key responsibility areas (KRAs) are the major outputs which the position is responsible and are not a comprehensive statement of the position activities.

• Adhere to ISO/IEC 17025, OECD Principles of GLP, GCLP Principles, 360biolabs' Quality Management System, and other requirements as per NATA Accreditation and regulatory guidelines
• Maintain awareness of, and ensure compliance with, relevant International Standards and Guidelines

• Interpret clinical protocols and identify appropriate techniques/methods to use for delivery of a client study
• Provide protocol/synopsis related quotes, contracts to secure new business
• Liaise with colleagues and clients to ensure agreements (CDA, MSA), quotations and Work Orders are aligned and finalised to maintain and develop 360biolabs' market position
• Maintain awareness of the market and competitors to maintain and develop 360biolabs' market position

• Review reports on activities, revenues forecasts, timelines, scheduling conflicts when required
• Assist in the production of reports and presentations as required

Key Selection Criteria

• Bachelor of Science (Hons) or equivalent industry experience (Essential)

Experience / Knowledge / Attributes

• Excellent organisational and writing skills (Essential)
• Experience with database computer software and file management (Essential)
• Ability to work effectively as part of a team (Essential)
• Excellent analytical, interpersonal, verbal and written communication skills (Essential)
• Proficient in use of Microsoft Office, including Word, Excel, and Power Point (Essential)
• Knowledge of laboratory techniques, pharmacokinetic and pharmacodynamic assays (Desirable)
• Experience in the conduct of early stage clinical studies and in the processing and analysis of clinical samples (Desirable)
• High motivation and enthusiasm for medical research and drug development (Desirable)