Global Clinical Lead, Renal Cancer Therapeutics

il y a 4 jours

Liège, Belgique Telix Pharmaceuticals (EMEA) Temps plein

Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. **At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases.**You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.

**See Yourself at Telix**

The Global Clinical Lead will ensure the renal cancer therapeutic programs are founded on sound scientific decision-making and are able to be progressed efficiently and effectively towards commercial realization by generating clinical data to serve the requirements of both internal stakeholders and external stakeholders including, but not limited to regulatory authorities, healthcare professionals, patient groups, guidelines committees, payors, and pharmaceutical and business development collaborators.

The Global Clinical Lead will work closely in a matrix organisation with the respective Global Program Leads, Clinical Operations, Medical Affairs, Regulatory Affairs, Manufacturing, Business Unit Heads and other relevant cross-functional teams to advance Telix Group's assets towards the clinic. This will be undertaken via a deep working knowledge of the existing and future competitive landscape in uro-oncology.

**Key Accountabilities**:

- Lead development of clinical development plans for therapeutic assets in renal cancer
- 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

**Education and Experience**:

- Medical degree or PhD required
- Clinical experience in medical oncology required; Nuclear medicine or renal cancer experience is highly preferred
- 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
- Experience with regulatory submissions (e.g., IND, CTA) and interaction with regulatory agencies (e.g., FDA, EMA) is preferred

**Key Capabilities**:

- Willingness to travel domestically and internationally, as needed
- Strong understanding of uro-oncology
- Excellent negotiation, communication, and interpersonal skills, with the ability to build and maintain relationships with diverse stakeholders
- Self-motivated, goal-oriented, and able to work independently as well as collaboratively within cross-functional teams

At Telix, we believe **everyone counts**, **we strive to be extraordinary**, and **we pursue our goals with determination and integrity**. You will be part of an engaged and supportive group of colleagues who all have a shared** purpose: to help people with cancer and rare diseases live longer, better quality lives.**Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world.**We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.

Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

VIEW OUR RECRUITMENT PRIVACY POLICY HERE

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