Clinical Project Manager

About the Company

Telix Pharmaceuticals is a fast-growing radiopharmaceutical company with headquarters in Australia and offices in Belgium, Japan, Switzerland, and the United States. The organization is focused on precision medicine through targeted radiation and develops products aimed at improving life for people with cancer and rare diseases. The role supports the global rollout of an approved prostate cancer imaging agent and contributes to late-stage clinical programs in oncology and rare diseases.

Role Overview

The Clinical Project Manager will coordinate and oversee the daily execution of several early-phase regional clinical trials, from protocol planning and study launch through clinical study report completion. The position involves managing documents, budgets, safety, and quality while working with CROs, external vendors, and internal teams to keep studies aligned with GCP, SOPs, and FDA/ICH requirements. The role also requires quickly identifying issues, resolving project risks, and making sure deliverables are completed on time and within budget.

Key Responsibilities

• Guide multiple clinical studies through planning, startup, conduct, maintenance, and closeout.
• Handle trial operations across vendor selection, site feasibility, site selection, timelines, budgeting, resource planning, and vendor coordination.
• Provide daily study oversight for CROs, vendors, and investigational sites in collaboration with cross-functional teams.
• Track external partner activities to ensure service quality stays aligned with agreed timelines and budgets.
• Contribute to the preparation, review, and updates of clinical development documents such as protocols, informed consent forms, investigator brochures, laboratory manuals, and IMP handling manuals.
• Ensure each trial has an effective operational project plan and follows the relevant SOPs.
• Spot risks early and use strong problem-solving skills to keep study issues moving toward resolution.
• Coordinate or monitor project work such as site monitoring and audits, CRF and database updates, data collection, patient safety and adverse event handling, document control, statistical analysis, final report preparation, and study closeout.
• Lead small to medium projects or provide regional leadership for complex multicenter studies.
• Maintain oversight of the study Trial Master File and support periodic TMF audits.
• Carry out additional duties as assigned by management.

Experience and Qualifications

A bachelor’s degree in life sciences is required, along with at least 2 years of relevant clinical trial project management experience. Strong knowledge of clinical trial operations is needed, and prior exposure to early-phase studies, oncology, or radiopharmaceutical programs is preferred. Candidates should be comfortable managing multiple priorities on tight timelines and should understand ICH GCP, drug development, clinical research practices, and regulatory processes. The role also calls for strong analytical, organizational, planning, decision-making, negotiation, and conflict-management abilities, plus the ability to build productive relationships with internal teams, vendors, and study sites. Fluency with Microsoft Office tools and working knowledge of CTMS and eTMF platforms are expected. Regional startup experience, including site feasibility and ethics/regulatory submissions, is preferred, along with the ability to shift strategy quickly in a fast-paced setting. Experience in conflict resolution, project finance awareness, and practical clinical project risk management is also valued.

Key Capabilities

• Inclusive approach to teamwork and respect for diversity
• Creative and practical problem-solving
• High standards and a strong focus on quality
• Results-driven mindset
• Ethical conduct and integrity
• Flexibility in changing environments
• Clear and confident communication
• Collaborative team orientation
• Resilience under pressure
• Commitment to ongoing learning and growth

Benefits

• Competitive pay
• Annual performance-based bonus
• Equity-based incentive program
• Generous vacation allowance
• Paid wellness days
• Learning and development support

Equal Opportunity

Telix Pharmaceuticals is an equal opportunity employer and considers qualified applicants without discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other protected characteristics.

Work Arrangement

This is a remote role based in the United States. The company also supports hybrid and remote employees across multiple global locations.