Clinical Trial Administrator

工作内容

#LI_TS

Novotech is internationally recognized as the leading regional full-service contract research organization (CRO) in Asia-Pacific providing clinical development services across all clinical trial phases and therapeutic areas, including an in-house and integrated global product development and regulatory affairs consultancy, BioDesk.

Working in a fast paced and adaptable environment, we set a high benchmark for clinical trial operations by listening carefully, allocating Asia Pacific’s best people and talent, and leveraging best in class platforms, technology, systems and processes to meet our client’s clinical program goals and ultimately improve patient lives.

Our people are critical in meeting organisational and client’s objectives and we place a strong emphasis on creating an inclusive, collaborative, transparent and collegiate work environment where everyone is supported to be the best they can be. We support our employees with financial assistance to enable flexible working arrangements, paid parental leave for primary and secondary careers, and regular training, learning, and international knowledge-sharing opportunities.

About The Position

We have an exciting new opportunity and are seeking a committed, adaptable and driven individual looking to build a career as a Clinical Trial Assistant based in Taiwan.

This role has been designed specifically for an individual interested in building a career in clinical trials project administration and coordination, but not seeking a CRA role. The Clinical Trial Assistant is a key member of the project team and the role has an established professional career path for high performers.

Core Responsibilities

On a day to day basis the CTA provides pivotal in-house administrative and operational support to Clinical Research Associates and Project Managers on Novotechs clinical trials. Key responsibilities include IRB submission, assisting clinical staff in the collection and maintenance of essential documents, management of the trial master file, attending meetings and taking minutes, tracking of study progress and management of the distribution of studies supplies.

Other Required Skills

• Minimum 2 years of administrative experience within Life Science of Healthcare organization
• Previous experience in Pharmaceutical, CRO or Healthcare industry would be preferable
• Advanced computer literacy including Word & Excel
• Excellent communication skill both in written and spoken English
• Strong attention to details, ability to meet deadlines and manage time & workflow effectively
  

Find out more about working at Novotech at: www.novotech-cro.com/careers

Novotech is committed to offering Equal Employment Opportunities (EEO) where everyone has equal access to employment opportunities based on merit, without fear of discrimination or harassment.