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The core responsibility for this position is as a member of Novotech’s Data Management group.
The Clinical Data Manager’s (CDM’s) role is to control all aspects of data management and to ensure compliance with Good Clinical Data Management Practices (GCDMP).
Member of the project team reporting to the Project Manager for integrated projects, the Clinical Data Manager is responsible for planning, conducting and managing of all aspects of data management for a clinical trial according to the client specifications, protocol, project plan, Data Management Plan, relevant GCDMP guidelines, regulatory requirements and SOPs.
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Graduate in a clinical or life sciences related field.
At least six to ten years experience in a similar role working in the 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.
Global clinical research services for biotech drug development.
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