Responsibilities:
- Main responsibilities: Be responsible for the reception, counting, labeling and verification of specimens, and ensure the accurate input of specimen information into the system as well as the effective distribution of specimens.
- Secondary work: Assist in assembling and inspecting the sampling and testing kits to ensure quality control.
- Document Management: Responsible for the scanning and archiving of documents related to the management of case specimens.
- Environmental maintenance: Keep the sample management area clean and orderly.
- Teamwork: Complete other related tasks assigned by the supervisor.
Personal trait requirements:
- Carefulness and patience
- Strong sense of responsibility
- Good English proficiency (TOEIC 550 or above, IELTS 4.5 or above or equivalent level)
- Teamwork spirit and good logical thinking
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.
