Job Description

:About the position:
We have an exciting new opportunity in our Project Management Group and are seeking a committed, adaptable and driven individual with administration experience who is looking to build a career as a Project Specialist (PS). The Project Specialist (PS) will support the Project Manager (PM) to complete study activities in accordance with local regulation, ICH GCP guidelines, and Novotech/client SOPs to deliver the project on time and to budget. The Project Specialist is a key member of the Project Support Team, and the role has an established professional career path for high performers.Required Professional Experience and Qualifications

• Graduate in a Clinical or Life Sciences related field and ideally 1- 2 years\' experience within the clinical research industry. Experience working in the pharmaceutical, CRO or healthcare industry would be advantageous.
• Previous experience in a Clinical Trial Administrator (CTA) role would be highly regarded.
• Superior written and verbal communication skills.
• Highly proficient in computer programs including Microsoft Office and experience with managing multiple databases.
• Excellent attention to detail with a strong focus on reaching a quality outcome.
• Demonstrated ability to meet deadlines and manage time and high-volume workflow effectively
• A proactive approach to work and a willingness to help improve inefficiencies.
• An ability to work flexibly as part of a team and with a variety of internal and external customers.

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 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 contacting you regarding your application.About Us: Novotech has offices in 11 geographies across the region, and site partnerships with key medical institutions.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.About the Team: Novotech is a leading Asia-Pacific biotech specialist CRO and consists of two operating brands, Novotech and PPC. Novotech is a clinical CRO with labs, phase I facilities, and drug development consulting services.It has accumulated experience in over 3,700 clinical projects, including Phase I to Phase IV clinical trials and bioequivalence studies. Novotech is positioned to serve biopharmaceutical clients conducting clinical trials in Asia and globally.As of September 30, 2021, Novotech had over 2,750 FTEs across 11 geographies in Asia-Pacific, the United States and the UK.

Novotech