Clinical Research Associate
3 weeks ago
**The Position**
Acting as the primary link between sites and sponsor, you will be responsible for:
- Acting as a site manager to ensure that clinical trials are conducted and documented as per ICH GCP guidelines, global and local regulatory requirements and Novotech/Client SOPs;
- Providing mentorship to less experienced staff;
- Providing support to the project manager as required; and
- Performing site selection visits to ensure sites have adequate resources to conduct studies.
**Minimum Qualifications & Experience**:
- At least 2 years of independent Oncology experience;
- Tertiary qualifications in clinical or life sciences related field (relevant experience/qualifications in similar professions may also be considered);
- 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.
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.
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