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Telix Pharmaceuticals Limited एक वाणिज्यिक चरण की जैव-औषधि कंपनी है, जो कैंसर और दुर्लभ रोगों के लिए थेरानोस्टिक रेडियोफार्मास्यूटिकल्स विकसित और व्यावसायीकृत करती है। इसका दृष्टिकोण लक्षित इमेजिंग को विकिरण-आधारित उपचार के साथ जोड़ता है, ताकि अधिक सूचित नैदानिक निर्णय और व्यक्तिगत देखभाल में सहायता मिल सके।
कंपनी की पाइपलाइन में प्रोस्टेट और किडनी कैंसर, न्यूरो-ऑन्कोलॉजी और मस्कुलोस्केलेटल कैंसर शामिल हैं। Telix ने अपने प्रमुख इमेजिंग उत्पाद Illuccix® के लिए वैश्विक नियामकीय अनुमोदन प्राप्त किए हैं और दुनिया भर में क्लिनिकल परीक्षणों के व्यापक कार्यक्रम को आगे बढ़ाना जारी रखा है। इसकी टीम स्वास्थ्य सेवा, जैव-प्रौद्योगिकी और संबंधित वाणिज्यिक क्षेत्रों में मिलकर काम करती है, ताकि रेडियोफार्मास्यूटिकल नवाचारों को विकास से क्लिनिकल उपयोग तक पहुंचाया जा सके।
Senior Clinical Project Manager, Remote (United States)
Lead global clinical trials for Telix Pharmaceuticals’ precision radiopharmaceuticals, overseeing study delivery from protocol finalization through closeout. Coordinate vendors, budgets, risks, and cross-functional teams across complex multinational research projects.
विवरण
- Oversee national and global clinical trials from protocol finalization through closeout.
- Select vendors and sites, assess feasibility, and manage timelines, budgets, resources, and vendor relationships.
- Forecast spending and identify ways to accelerate work or shift expenditure.
- Create integrated study management plans with the core project team.
- Prepare and maintain study documents, including protocols, informed consent forms, and clinical manuals.
- Track external partners’ quality, timelines, and budget performance.
- Put effective project plans into operation in line with applicable SOPs.
- Anticipate and manage risks, leading teams through problem-solving and resolution.
- Help develop and maintain clinical SOPs and trial processes.
- Shape project delivery strategies for RFPs and lead bid defense preparation.
- Direct complex, multinational, multicenter clinical research projects.
- Create patient recruitment strategies.
- Negotiate site and vendor contracts and budgets.
- Update leadership and cross-functional stakeholders on trial progress, issues, and mitigations.
- Train study team members and mentor clinical project managers.
- Work independently with limited supervision.
- Represent clinical operations at medical conferences through investigator engagement and presentations.
आवश्यकताएँ
- A bachelor’s degree in life sciences is required.
- PMP certification is preferred.
- At least five years of relevant clinical trial project management experience is required.
- Experience with late-phase trials (Phase 3–4 or registration studies), oncology, and/or radiopharmaceuticals is preferred.
- Strong written and verbal communication, organization, and problem-solving skills, including the ability to meet tight timelines.
- Collaborative approach and ability to work across functions.
- Experience managing global clinical trials.
- Thorough knowledge of ICH Good Clinical Practice (GCP) and regulatory processes.
- Ability to quickly adjust study strategy and guide teams effectively.
- Strong analytical, organizational, planning, decision-making, negotiation, and conflict-management skills.
- Proficiency with Microsoft Office, including Word, Excel, SharePoint, and Teams, and experience working primarily with electronic records.
- Demonstrated leadership and ability to support others’ development.
- Study startup experience, including country and site feasibility and ethics and regulatory submissions across multiple regions (APAC, EMEA, and North America).
- Travel of approximately 10% is expected.
लाभ
- Competitive salary.
- Annual performance-based bonuses.
- Equity-based incentive program.
- Generous vacation.
- Paid wellness days.
- Learning and development support.
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