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The project Manager is primarily responsible for the planning and management of all
contracted responsibilities for assigned projects and to act as the primary
contact between Novotech and its clients.
Responsibilities
Determine project feasibility, considering
the needs of the sponsor as required to assist Business Development.
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.
Work with the Vendor Manager to assess,
appoint and manage study vendors to ensure the study is adequately supported,
e.g. central laboratory, drug distributors, IRT providers.
Coordinates workstream and cross functional
project teams, such as Clinical, Regulatory, Medical, Biometrics and
Pharmacovigilance.
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,
including Associate Project Manager or equivalent.
English is fluent