🌍 Position Title: Global Clinical Lead (Clinical Scientist)
Location: Canada – Remote
Company: Telix Pharmaceuticals
Updated On: Thursday, 23 October 2025
🏢 About Telix Pharmaceuticals
Telix Pharmaceuticals is a global, 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, improving quality of life for people living with cancer and rare diseases.
You will be part of the team supporting the international roll-out of our approved prostate cancer imaging agent and advancing our late-stage oncology and rare disease portfolio.
🎯 Role Overview
The Global Clinical Lead is responsible for the end-to-end clinical development of novel imaging agents within the FAP (Fibroblast Activation Protein) program.
You will ensure that clinical strategy is scientifically robust, commercially aligned, and that clinical studies generate data supporting regulatory approval, market access, and adoption.
You will collaborate across Global Program Leads, Clinical Operations, Medical Affairs, Regulatory, Manufacturing, and Commercial teams in a matrixed, cross-functional environment.
⚙️ Key Responsibilities
1. Clinical Strategy Development
Define and lead clinical development plans for FAP imaging assets.
Align with Telix’s global asset and commercial strategies.
2. Cross-Functional Collaboration
Work closely with Global Program Heads, Regulatory Affairs, Medical Affairs, and Translational Medicine.
Ensure integration of clinical trial objectives with business and scientific goals.
3. Clinical Study Design & Execution
Oversee clinical study plans from concept to protocol finalization.
Maintain scientific rigor and regulatory alignment.
Incorporate inputs from healthcare providers, patient advocacy groups, and payors.
4. Clinical Documentation Leadership
Lead preparation and review of:
Informed consent forms
Imaging charters
Study manuals
Regulatory dossiers and related documentation
5. Regulatory & Scientific Contributions
Provide clinical input to regulatory and scientific documents such as:
Investigator Brochures, IMPDs, DSURs, PSURs, SUSARs, CSRs
IND, BLA, NDA, and MAA submissions
6. Data Analysis & Quality Review
Oversee review and interpretation of efficacy, safety, and imaging data.
Ensure integrity and reliability of clinical data across all phases.
7. Stakeholder Communication
Deliver presentations, proposals, and progress reports to senior leadership and external collaborators.
8. External Engagement & Thought Leadership
Build strong relationships with Key Opinion Leaders (KOLs) and advisory boards.
Engage consultants and subject matter experts to refine clinical strategy.
🎓 Education & Experience
|
Requirement |
Details |
|---|---|
|
Qualification |
MD or PhD in a relevant scientific discipline |
|
Therapeutic Area Expertise |
Oncology or Nuclear Medicine (mandatory) |
|
Experience |
Minimum 5 years in clinical development, with proven leadership of early-phase programs |
|
Regulatory Knowledge |
Understanding of global clinical trial methodologies, regulatory frameworks, and submissions (e.g., INDs, CTAs) |
|
Leadership |
Experience leading cross-functional teams and managing clinical programs end-to-end |
|
Scientific & Strategic Skills |
Strong grasp of clinical trial design, data interpretation, and strategic development |
💡 Key Capabilities
✈️ Willingness to travel domestically/internationally as required
🌈 Inclusive mindset and respect for diversity
💭 Creative problem-solving and innovative thinking
🏆 Commitment to excellence and results-oriented work ethic
⚖️ High ethical standards and integrity in all interactions
🔄 Adaptability in dynamic, fast-paced environments
🗣️ Strong communication and collaboration skills
💪 Resilience and ability to thrive through challenges
📚 Continuous learning and professional growth mindset
💼 Why Join Telix
Be part of a mission-driven global team advancing precision medicine.
Work in a hybrid or fully remote setup with global collaboration.
Competitive salary, annual performance bonuses, equity incentives, and wellness support.
Learning & Development programs to grow your professional potential.
Inclusive culture where everyone counts and integrity drives success.
⚖️ Equal Opportunity Statement
Telix Pharmaceuticals is an equal opportunity employer.
We evaluate all applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
🔗 Learn More: [Telix Pharmaceuticals LinkedIn Page]
📄 Privacy Policy: View on official website
📩 Apply Now: [Click Here to Apply]
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