Clinical Trial Specialist - Remote

Overview

Telix Pharmaceuticals is a dynamic, 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. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.

In Short

• The CTS will aid in new site onboarding, helping the site optimize settings and protocols to increase proper use of Telix radiopharmaceuticals in commercial setting and clinical trial setup.
• Align and execute field activities in support of Medical Affairs Strategic plan.
• Identify and communicate research gaps, opportunities, and relevant field intelligence to inform medical strategy.
• Identify opportunities for medical team to present education and publications on disease state, real world experience and clinical trials.
• Leverage expertise to enhance and broaden knowledge among internal and external stakeholders.
• Attend medical/scientific meetings to represent Medical Affairs by strengthen individual expertise/proficiency as well as capture, integrate, and summarize information of strategic interest.
• Appropriately support submission of Medical Education grants and Investigator-Initiated Research.
• Provide product training and presentations to internal and external stakeholders to ensure accurate communication and utilization of Telix products.
• Support cross-functional colleagues (e.g., commercial, marketing, clinical operations), in appropriate activities.
• Support new site onboarding to ensure successful first and subsequent scanning.

Requirements

• BS or MS degree in scientific discipline (preferred Radiology or similar) or equivalent experience required.
• Certification by Nuclear Medicine Technology Certification Board (NMTCB) or the American Registry of Radiologic Technologist (ARRT) required.
• 2 years’ experience with technical aspects of PET/CT scanning with NGI’s required.
• Experience in radiopharmaceuticals required, prostate cancer preferred.
• Thorough understanding of relevant policies guiding the Pharmaceutical Industry.
• Experience/expertise in interpretation of scientific data, market research, and competitive intelligence tools.
• Proficient in Microsoft Office Suite.
• Excellent verbal and written communication skills.
• Strong multi-tasking, time-management, organization and interpersonal skills, business acumen, and high level of emotional intelligence.
• Detailed knowledge of regulations and practices related to industry interactions with healthcare professionals.

Benefits

• Competitive salaries.
• Annual performance-based bonuses.
• Equity-based incentive program.
• Generous vacation.
• Paid wellness days.
• Support for learning and development.