About the role
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality.
Responsibilities
- Follow the assignment and direction by director of department.
- Site Start-up.
- Project Execution and Management.
- Data entry and management.
Experience and Qualifications
- College above, graduated in Medicine, Nursing, and Pharmacology related departments graduation.
- Provided with knowledge of GCP.
- Good command of English. Familiar with office and Project software.
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.
