Major Responsibilities
- Conduct analysis work following related SOPs and guidance.
- Draft/check/review/approve documents, such as SOP, protocol, analytical result, report and method.
- Involve in lab logistics (general affair) management, such as purchasing, inventory controlling, payment applying.
- Responsible for instrument maintenances, workspace cleaning/maintenance.
- Delegated/assigned as the system owner for computerized system, do the corresponding work for system, such as validation test, periodic review, report, etc.
- Participate in CAP/GCP/GLP/regulatory related training courses.
- Provide temporary supporting assigned by line manager.
- Involve in sample collection kit/label preparation.
- Involve in analytical study project management.
- Refer to additional Study Based Responsibilities while being assigned in GLP project.
Qualifications & Experience Education
- A 4-year BS (Bachelor of Science) degree in Biochemistry, Biotechnology and Laboratory Science, Chemistry, or a related field. Or Junior colleague with over 3-year lab work experience and well qualified. Advanced degree is a plus for Associate Researcher/ Senior Researcher.
- License of Medical Technician is required for Associate Researcher/ Senior Researcher in Central Lab.
Knowledge, Skills, and Abilities
- Familiar with all lab operation activities.
- Excellent working knowledge of CAP/GCP, applicable law (local and country) and regulatory requirements.
- Good communication skills.
- Good verbal and written English or other second language skills.
- Good problem-solving skills.
- Effective time management and prioritization skills.
Experiences
- Prefer with over 3-year lab work experience and well qualified.
Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.
Our team members are passionate about what we do, but we understand work is only one of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.
We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.
We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to talking to you about working at Novotech.
Novotech is a global full-service clinical Contract Research Organization (CRO).
Headquartered in Sydney, Australia, Novotech has 34 offices across Asia-Pacific, North America, and Europe. Novotech employs over 3000 employees and has over 5000 site partnerships and the resources and infrastructure to scale regionally and globally as clinical programs advance.
Novotech provides clinical development services across all clinical trial phases and therapeutic areas including feasibility assessments, ethics committee and regulatory submissions, data management, statistical analysis, medical monitoring, safety solutions, central lab services, report write-up to ICH requirements, project and vendor management. Novotech obtained the ISO 27001 certification which is the best-known standard in the ISO family providing requirements for an Information Security Management System. Together with the ISO 9001 Quality Management system, Novotech aims at the highest IT security and quality standards for patients and biotechnology companies.