Full-Time Sr. Global Clinical Lead, Prostate Cancer Imaging
Telix Pharmaceuticals (Americas) is hiring a remote Full-Time Sr. Global Clinical Lead, Prostate Cancer Imaging. The career level for this job opening is Experienced and is accepting Canada based applicants remotely. Read complete job description before applying.
Telix Pharmaceuticals (Americas)
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Telix Pharmaceuticals is seeking a dynamic and experienced Sr. Global Clinical Lead in Prostate Cancer Imaging as part of our Clinical Strategy and Innovation team. The successful candidate will be responsible for designing and executing clinical trials for novel radiopharmaceutical products in prostate cancer imaging.
The Sr. Global Clinical Lead will ensure the prostate cancer imaging programs are founded on sound scientific decision-making and are able to be progressed efficiently and effectively towards commercial realization. This will be undertaken via a deep working knowledge of the existing and future competitive landscape in prostate cancer.
Key Accountabilities:
- Lead development of clinical development plans for imaging assets in prostate 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
- Lead clinical scientific input into documentation including investigator brochures, IMPDs, safety reports
- Lead the analysis, review, and quality control of clinical data
- Prepare and deliver presentations, proposals, and reports for senior management, partners, and other stakeholders
Education and Experience:
- PhD or Medical degree required
- Clinical experience in medical oncology or nuclear medicine is essential
- 7+ years of experience in clinical development required
- 5+ years leading high functioning global matrix teams required
- Strong knowledge of clinical trial design, methodology, and regulatory requirements required
- Experience with regulatory submissions (e.g., IND, CTA) and interaction with regulatory agencies (e.g., FDA, EMA) is preferred
Key Capabilities:
- Inclusive mindset
- Creativity and innovation
- Commitment to excellence
- Results-oriented
- Ethical behavior
- Adaptability
- Strong communication skills
- Collaboration
- Resilience
- Continuous learning