Project Manager, TLX250Px

Scorpion Therapeutics; United States; Hybrid; USD 90,000 - 150,000; Full time

Job summary

Telix Pharmaceuticals is seeking a Project Manager to support radiopharmaceutical development and commercialization, including international rollout and late-stage oncology products. You will oversee planning, budgeting, scheduling, and risk management, ensuring timely, within-budget delivery on global programs.

Work with clinical, regulatory, manufacturing, supply chain, and quality teams across regions. The role requires PM experience in pharma/biotech and proficiency with SmartSheet, with a

Qualifications

• Postgraduate degree in science or life sciences.
• 2+ years in pharma/biotech, with preclinical and clinical development (Phase 1-3).
• Proven PM experience on multiple small projects or a complex program.
• Expertise in at least one development function (clinical ops, manufacturing, regulatory, or non-clinical).
• Experience with project management software (SmartSheet preferred).

Responsibilities

• Oversee all project aspects—from planning, budgeting, scheduling to risk management—ensuring timely and within-budget delivery.
• Facilitate cross-functional collaboration with clinical, regulatory, manufacturing, supply chain, and quality teams.
• Maintain project management tools and data accuracy.
• Track financials and vendor activities.
• Lead risk and change management processes; and
• Report progress to stakeholders.

Skills

Cross-functional leadership

Risk management

Education

Postgraduate degree in life sciences

Tools

SmartSheet

Job description

Role: Project Manager supporting Telix Pharmaceuticals' radiopharmaceutical development and commercialization efforts, including international rollout and late-stage oncology products.

Responsibilities:

• oversee all project aspects—from planning, budgeting, scheduling to risk management—ensuring timely and within-budget delivery.
• Facilitate cross-functional collaboration with clinical, regulatory, manufacturing, supply chain, and quality teams;
• maintain project management tools and data accuracy;
• track financials and vendor activities;
• lead risk and change management processes; and
• report progress to stakeholders.

Qualifications:

• postgraduate degree in science or life sciences;
• 2+ years of industry experience in pharmaceutical or biotech sectors, particularly with preclinical and clinical development (Phase 1-3);
• proven project management experience with multiple small projects or a complex project;
• expertise in at least one pharmaceutical development function such as clinical operations, manufacturing, regulatory, or non-clinical development;
• experience with project management software (SmartSheet preferred).

High-Value:

focus on oncology, radiopharmaceuticals, late-stage clinical development, cross-functional team leadership, project and financial management.

Work setup:

hybrid or remote, with a global and interdisciplinary team; travel not explicitly specified.