Senior Clinical Project Manager

🕒 March 4

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Logo of Telix Pharmaceuticals Limited

Telix Pharmaceuticals Limited

501 - 1000 employees

Founded 2015

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Telix Pharmaceuticals Limited is a commercial-stage biopharmaceutical company dedicated to transforming the way cancer and rare diseases are diagnosed and treated. Focusing on the development and commercialization of theranostic radiopharmaceuticals, Telix utilizes targeted radiation to enhance treatment decision-making and deliver personalized therapy. With an extensive pipeline addressing areas such as prostate and kidney cancer, neuro-oncology, and musculoskeletal cancers, Telix has garnered global regulatory approvals for its lead imaging agent, Illuccix®, and is actively conducting numerous clinical trials worldwide.

📋 Description

• Proactively managing all aspects of the trial process including vendor selection, site feasibility and selection, trial timelines, budgets, resources, and vendor relationships from protocol finalization through to study closeout. • Forecast and identify opportunities to accelerate activities to bring spend forward or identify if spend will shift. • Independently develop integrated study management plans with the core project team. • Developing and managing all study-related documents such as study protocol, informed consent, clinical manuals, and implementing quality standards. • Monitoring all work performed by the external partners to ensure quality of the service with respect to mutually agreed timelines and budget. • Ensuring effective project plans are in place and operational for each trial within trial appropriate SOPs. • Managing risks proactively and leading problem solving and resolution efforts • Support the development and maintenance clinical SOPs & trial process’ as required. • Developing project delivery strategy for RFPs. Lead in bid defense preparations. Understand project strategy and translate the agreed upon approach. • Management of complex multi-national, multi-center clinical research projects • Develop patient recruitment strategies • Conduct contract and budget negotiations with sites and vendors • Communicate trial status, issues, and mitigations to leadership and relevant cross-functional stakeholders • Train study team members and act as mentor for CPMs • Work independently with limited supervision • Attend medical conferences and represent clinical operations through investigator engagement and/or presentations

🎯 Requirements

• Bachelor’s degree in life sciences required, PMP preferred • 5+ years of relevant experience in Clinical Trial Project Management required • Experience with late phase clinical trials (Phase 3 - 4, registration trials), oncology and/or radiopharmaceutical experience preferred. • Excellent oral and written communication, organizational, and problem-solving skills while working under strict timelines. • Team oriented mindset and demonstrates ability to work with cross functional teams. • Experience managing global clinical trials. • Thorough knowledge of ICH Good Clinical Practice (GCP) and regulatory processes. • Demonstrated ability to pivot study strategy quickly and lead teams in the right direction. • Strong analytical, organisational, planning, decision making, negotiation, and conflict management skills. • Fluent in Microsoft Office suite (Word, Excel, SharePoint, Teams, etc.) and experienced in working in mainly electronic record-keeping environment. • Demonstrated leadership skills and ability to cultivate development of others • Start-up experience (country and site feasibility, ethics & regulatory submissions in multiple regions (APAC, EMEA, NA))

🏖️ Benefits

• Competitive salaries • Annual performance-based bonuses • Equity-based incentive program • Generous vacation • Paid wellness days • Support for learning and development

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