Clinical Research Associate II - Clinical Research Associate III-Senior CRA

工作内容

Job Description

Novotech is internationally recognised as the leading independent and full service contract research organisation (CRO) in the Asia Pacific region. We provide a wide range of clinical development services across all research phases and therapeutic areas; and have been instrumental in the success of hundreds of Phase I – IV clinical trials throughout the Asia Pacific.

Powered by the highest quality people, Novotech strives to set the benchmark for both business and clinical trial performance.

Our people are one of our key strengths. We value our people and recognise the work they do. We are lucky to have the best people and talent from across the Asia Pacific region work together to deliver to clinical trial success for our clients.

Our people and those we look to recruit have an attitude of making things happen. They are problem solvers, driven with a focus on delivering quality, accountability and a high level of performance.

About The Position

We are currently seeking committed, adaptable and driven individuals for Clinical Research Associate office-based position based in Taiwan.

Core Responsibilities

The core focus of the CRA role is to ensure the rights and the wellbeing of the trial participants are protected and the reported trial data is accurate, complete and verifiable from source documents. The CRA is also the primary link between Investigational sites and Sponsor, acting as a site manager ensuring that clinical trials are conducted and documented as per ICH GCP guidelines, global and local regulatory requirements and Novotech/Client SOP’s.

Required Qualification(s)

• Tertiary qualifications in clinical or life sciences related field (relevant experience/qualifications in similar professions may also be considered);
  

Required Professional Experience

This role will be based in our Taiwan office, ideal candidate will have:

• At least 2-3 years of independent CRA experience;
• Solid knowledge of GCP, national and international regulations and a sound understanding of how they apply to you;
• Excellent interpersonal and team skills with a genuine commitment to contributing to the development of innovative treatments;
• Previous experience in monitoring oncology trials would be highly desirable; and
• A strong track record of performing visits to sites according to the Clinical Monitoring Plan.
  

Opportunities And Benefits

To deliver clinical trial and research excellence for our clients, our people are ’best in class’.

At Novotech, we seek and nurture people with exceptional talent. We are committed to providing our people with regular internal and external training, a competitive bonus structure and a supportive work environment.

We are also focused on providing our people with a wide variety of career growth and development opportunities.

For more information about where your next career step at Novotech might take you, visit http://novotech-cro.com/novotech-careers