Global Clinical Lead

Summary

Join Telix Pharmaceuticals, a global radiopharmaceutical company, as their experienced Global Clinical Lead. You will be responsible for designing and executing clinical trials for novel radiopharmaceutical products, focusing on solid tumors. This role requires a PhD or Medical degree, 5+ years of clinical development experience, and strong knowledge of clinical trial design and regulatory requirements. You will collaborate with various teams to advance Telix's assets towards the clinic and contribute to the development of clinical study documentation. The position offers a unique opportunity to drive cutting-edge clinical development strategy in areas of high unmet need and is part of a supportive, global team. Telix offers competitive salaries, bonuses, equity incentives, generous vacation, paid wellness days, and support for learning and development.

Requirements

• PhD or Medical degree required
• Experience in medical oncology or nuclear medicine is required
• 5+ years of experience in clinical development required
• Strong knowledge of clinical trial design, methodology, and regulatory requirements
• Successful leadership and project management of clinical development programs

Responsibilities

• Lead development of clinical development plans
• Collaborate with global program heads, regulatory affairs, medical affairs, and translational medicine teams to ensure alignment of clinical trial objectives with overall asset strategy
• Develop clinical study plans from concept to synopsis to full protocol, ensuring alignment with the Company’s objectives, and the needs of regulatory authorities, healthcare professionals, patient groups, guidelines committees and payors
• Develop – in collaboration with relevant cross-functional teams and medical writers – clinical study documentation including, but not limited to informed consent documents, imaging charters, study manuals and final regulatory dossiers
• Lead clinical scientific input into documentation including investigator brochures, IMPDs, safety reports (e.g. DSURs, PSURs, and SUSARs), clinical study reports and regulatory documents such as briefing packages, INDs, BLAs, NDAs and MAAs
• Lead the analysis, review, and quality control of clinical data (e.g. study-related, aggregated) including efficacy, safety, and imaging data to ensure accuracy and quality
• Prepare and deliver presentations, proposals, and reports for senior management, partners, and other stakeholders

Preferred Qualifications

Experience with regulatory submissions (e.g., IND, CTA) and interaction with regulatory agencies (e.g., FDA, EMA) is preferred

Benefits

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