Clinical Data Associate

About the Role

The Clinical Data Associate supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs

Responsibilities:

• Data entry of clinical trial data using Clinical Data Management software.

• Assistance in review of data queries to be raised with sponsor companies/monitoring

• staff.

• Tracking of CRF pages received and entered, tracking of data queries sent received

• and entered.

• Assist CDM with database testing and edit checks testing as appropriate.

• Assist CDM with data cleaning/validation and reconciliation of external data

• Develop and maintain good communications and working relationships with lead

• CDMs.

• Assist CDM to create reports, listings, and other output as required during the course of the project

Experience and Qualifications:

• Graduate in a clinical or life sciences related field.

• Relevant experience /qualifications in allied professions may also be considered.

• Preferably at least six months to one year experience working in a data management role within research, pharmaceutical industry or a related field.

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.