Project Manager

at  Novotech

EXPERIENCE AND QUALIFICATIONS

• Graduate in a clinical or life sciences related field.
• Relevant experience/qualifications in allied professions may also be considered.
• At least 5 years’ experience within the clinical research industry and previous project management experience.
• CRO experience is advantageous as is experience with gene therapy
• Experience in Net Suite will be added advantage.
  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 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 contacting you regarding your applicatio

ABOUT THE ROLE

Project Managers are responsible for the delivery of the project from site selection through to the close out phase (including the CSR if applicable). The Project Manager is responsible for identifying and evaluating potential risks and to develop risk management plans to mitigate this risk.
Do you have Clinical Research experience and worked on gene therapy?

RESPONSIBILITIES

• Determine project feasibility, considering the needs of the sponsor.
• Actively provide guidance and review scope of work, responsibilities, timelines and quality of deliverables.
• Understand the requirements of the Project Agreement and ensure Novotech performs these services to the required standards.
• Understand the inherent risks of the project and collaborate with management to ensure appropriate contingencies are initiated.
• Ensure set up and maintenance of operational project plans, timelines & study tracking tools (such as CTMS), and eTMF, as required.
• Assess, appoint and manage study vendors to ensure the study is adequately supported, e.g. central laboratory, drug distributors, IVRS providers.
• Coordinate workstream and cross functional project teams, such as Clinical, Regulatory, Medical, Biometrics and Pharmacovigilance