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Senior Clinical Project Manager

10 hours, 36 minutes ago
United States
Full-time
Senior
Project Manager
Project and Program Management
Apply Now
Telix Pharmaceuticals

Telix Pharmaceuticals

Telix Pharmaceuticals is a global biopharmaceutical firm dedicated to the development and commercialization of diagnostic and therapeutic products that utilize targeted radiation, aiming to enhance treatment decisions and provide personalized therapies...

Pharmaceuticals
201-500
Founded 2015
View All Jobs 31

Description

  • Manage clinical trials from protocol finalization through study closeout, including timelines, budgets, resources, vendors and sites.
  • Develop integrated study management plans and ensure trial plans operate in accordance with applicable SOPs.
  • Develop and manage study documents, including protocols, informed-consent forms and clinical manuals, while implementing quality standards.
  • Oversee external partners to ensure services meet agreed quality, timeline and budget expectations.
  • Proactively identify, manage and resolve study risks and project issues.
  • Lead multinational, multicenter clinical research projects and develop patient recruitment strategies.
  • Conduct contract and budget negotiations with sites and vendors.
  • Develop RFP delivery strategies and lead bid-defense preparation.
  • Communicate trial status, issues and mitigation plans to leadership and cross-functional stakeholders.
  • Train and mentor study team members and Clinical Project Managers; represent Clinical Operations at medical conferences and investigator engagements.

Requirements

  • Bachelor’s degree in life sciences required; PMP certification preferred.
  • 5+ years of relevant clinical trial project management experience.
  • Experience managing global clinical trials and complex multinational, multicenter studies.
  • Experience with late-phase Phase 3–4 or registration trials; oncology and/or radiopharmaceutical experience preferred.
  • Knowledge of ICH Good Clinical Practice and regulatory processes.
  • Clinical start-up experience, including country and site feasibility and ethics and regulatory submissions across APAC, EMEA and North America.
  • Strong communication, organization, analytical, planning, decision-making, negotiation and conflict-management skills.
  • Demonstrated leadership, team development, cross-functional collaboration and ability to adapt study strategy quickly.
  • Proficiency with Microsoft Office, including Word, Excel, SharePoint and Teams, and electronic record-keeping environments.
  • Ability to work independently under strict timelines and travel approximately 10%.

Benefits

  • Competitive salary.
  • Annual performance-based bonus.
  • Equity-based incentive program.
  • Generous vacation and paid wellness days.
  • Learning and development support.
  • Hybrid and remote work opportunities.
  • Supportive global, interdisciplinary team environment.

Interested in this position?

Apply directly on the company website

Apply Now

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