Associate Clinical Data Manager at Novotech
Australia, , Australia -
Full Time


Start Date

Immediate

Expiry Date

10 May, 25

Salary

0.0

Posted On

11 Feb, 25

Experience

3 year(s) or above

Remote Job

No

Telecommute

No

Sponsor Visa

No

Skills

Gender Equality, Clinical Research, Development Programs, Pharmaceutical Industry

Industry

Pharmaceuticals

Description

EXPERIENCE AND QUALIFICATIONS:

  • Graduate in a clinical or life sciences related field.
  • At least three to six years experience working in a Clinical Data Associate (or equivalent) role in a Pharmaceutical industry or related role..
    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
Responsibilities

ABOUT THE ROLE

As a member of the project team reporting to the Biometrics Project Manager, the Associate 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

RESPONSIBILITIES:

  • Perform comprehensive data management tasks including data review, query management, external data reconciliation
  • Design and review of database structure, validation rules and consistency checks.
  • Operation of Clinical Data Management software for data entry of clinical trial results.
  • All data cleaning/validation tasks
  • Development of all key Data Management Documents
  • Liaison with the project team and client for preparing and maintaining Data Management Plans
  • Supervision and training support for junior and contract Data Management staff as required.
  • Active contribution to company business development initiatives, including involvement in the implementation of data management plans for business development in the company in general.
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