Responsibilities
Performing site evaluation, initiation, monitoring and close-out visits, plus maintaining appropriate documentation according to a project-specific monitoring plan, ICH-GCP, and applicable regulations.
Supporting the development of a subject recruitment plan.
Establishing regular lines of communication plus administering protocol and related study training to assigned sites.
Evaluating the quality and integrity of site practices - escalating quality issues as appropriate.
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.
Assist of country and/or site start up activities, including but not limit to country/site ICF development, preparation of IRB submission package, site contract and budget negotiation, and regulatory documents collection.
Perform the tasks assigned by line manager.
Experience and Qualifications
BS (Bachelor of Science) degree or equivalence experience. Advanced degree is a plus.
At least 2.5 year experience in clinical research environment.
Good command of written and spoken in English, good organization and communication skills.
High attention to detail and accuracy.
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.
