Senior Oncology Project Manager – Hybrid Clinical Trials

Novotech; Sydney; Hybrid; AUD 110,000 - 150,000; Full time

Benefits offered by this job

Flexible working options

Paid parental leave

Wellness programs

Ongoing development programs

Circle Back Initiative Employer

Job summary

Novotech seeks an experienced Project Manager to lead clinical study delivery in Australia, working in a hybrid setup. You will coordinate cross-functional teams, manage scope, timelines and budgets, and ensure adherence to ICH GCP and regulatory standards.

The role requires a life sciences graduate with 5+ years in clinical research and project management; CRO experience is advantageous. You will liaise with sponsors, vendors and sites to drive study success and profitability.

Qualifications

• Graduate in a clinical or life sciences related field.
• At least 5 years of experience within the clinical research industry and previous project management experience.
• CRO experience is advantageous.

Responsibilities

• Determine project feasibility, considering sponsor needs to assist Business Development.
• Actively provide guidance and review scope of work, responsibilities, timelines and quality of deliverables.
• Understand project agreements, manage risks, contingencies and ensure required standards.
• Set up and maintain operational project plans, timelines and study tracking tools (CTMS, eTMF).
• Coordinate workstreams and cross-functional teams (Clinical, Regulatory, Medical, Biometrics, PV).
• Manage the study budget and revenue, ensure profitability and changes are approved with BD.
• Identify and manage investigational sites to meet objectives and timelines.
• Ensure site training, regulatory submissions, and Investigator Meetings.
• Maintain TMF and essential documents; coordinate IP receipt, storage and disposition.

Education

Graduate in a clinical or life sciences related field

Job description

Novotech seeks an experienced Project Manager to lead clinical study delivery in Australia, working in a hybrid setup. You will coordinate cross-functional teams, manage scope, timelines and budgets, and ensure adherence to ICH GCP and regulatory standards.

The role requires a life sciences graduate with 5+ years in clinical research and project management; CRO experience is advantageous. You will liaise with sponsors, vendors and sites to drive study success and profitability.