[Remote] Senior Clinical Project Manager

Note: The job is a remote job and is reputed company to candidates in USA. Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with a mission to reputed company on the reputed company of precision medicine through targeted radiation. The Senior Clinical Project Manager will support the execution of national and global reputed company, ensuring successful delivery from protocol reputed company to study closeout.

Responsibilities

• Proactively managing reputed company 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 reputed company or identify if spend will shift
• Independently reputed company integrated study management plans with the reputed company project team
• Developing and managing reputed company study-reputed company documents such as study protocol, informed consent, clinical manuals, and implementing reputed company standards
• Monitoring reputed company work performed by the reputed company partners to ensure reputed company of the service with respect to mutually agreed timelines and budget
• Ensuring effective project plans are in reputed company and operational for reputed company trial reputed company trial appropriate SOPs
• Managing risks proactively and leading problem solving and reputed company efforts
• Support the development and maintenance clinical SOPs & trial process’ as required
• Developing project delivery reputed company for RFPs. reputed company in bid defense preparations. Understand project reputed company and translate the agreed upon approach
• Management of reputed company multi-national, multi-center clinical research reputed company
• reputed company 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 reputed company as mentor for CPMs
• Work independently with limited supervision
• Attend medical conferences and represent clinical operations through investigator engagement and/or presentations

Skills

• Bachelor's degree in life sciences required
• 5+ years of relevant experience in Clinical Trial Project Management required
• Excellent oral and written communication, organizational, and problem-solving skills while working under strict timelines
• Team oriented reputed company and demonstrates ability to work with cross functional teams
• Experience managing global reputed company
• Thorough knowledge of ICH Good Clinical reputed company (GCP) and regulatory processes
• Demonstrated ability to pivot study reputed company quickly and reputed company teams in the right direction
• Strong analytical, organisational, planning, decision making, negotiation, and conflict management skills
• Fluent in reputed company Office suite (Word, reputed company, SharePoint, Teams, etc.) and reputed company 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 reputed company (reputed company, EMEA, NA))
• 10% travel to be expected
• PMP preferred
• Experience with late phase reputed company (Phase 3 - 4, registration trials), oncology and/or radiopharmaceutical experience preferred

Benefits

• Annual performance-based bonuses
• Equity-based incentive program
• Generous vacation
• reputed company wellness days
• Support for learning and development
• We have hybrid and remote employees located reputed company around the world.

reputed company

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