See Yourself at Telix

The Medical Director of the Prostate Cancer Theranostics will lead medical affairs leadership, strategy, commercial launch alignment and tactics across the prostate cancer theranostics portfolio in North America. Responsibilities include integration of strategic priorities and tactical alignment across complex organizational matrixes (Commercial, Clinical Operations, Marketing, etc.). Working with key organizational stakeholders to develop and execute the medical affairs plan, including, medical education, research grants, medical advisory boards, and scientific communication/publication components within the overall medical operating plan. This role is responsible for the execution and oversight of launch success for lifecycle management of prostate cancer imaging asset and therapeutic area while contributing as a key SME providing strategic input and liaise with external stakeholders to drive Telix’s overall medical and clinical value in the medical community.

Responsibilities

• With limited oversight lead US medical strategic planning, prioritization, and execution of prostate cancer medical activities. Align cross-functionally on objectives, deliverables, roles & responsibilities.
• Develop high-performing US medical team. Recruit, retain and develop outstanding MSLs. Establish, communicate, and systematically review performance expectations, and personal development plans.
• Build and lead medical affairs strategy for upcoming product launch in the prostate cancer space. Ensures alignment across all medical affairs tactics and deliverables for launch.
• In collaboration with Clinical Development, Commercial, Market Access, HEOR and other functional areas, provide SME for strategic input.
• Providing medical input into development, execution, and interpretation of clinical protocols. This includes review of draft independent research protocols, reports and manuscripts; support EAP, clinical registries and other post-marketing commitments.
• Assists in the development of scientifically accurate marketing materials, medical education programs, advisories, and symposia. Assists with the scientific review, development, approval, execution and communication.
• Act as the Medical Lead for designated clinical trials or programs. Engage with key opinion leaders and deliver scientific presentations during advisory boards.
• Support medinfo with SRL medical/scientific development.
• Interpret and effectively communicate data obtained from clinical trials. 

What You’ll Bring to the Role

• Advanced degree (PhD, PharmD, MD) with prostate oncology experience required or equivalent experience. 
• 4+ years Medical Affairs experience and 2+ years of management experience.
• Experience working with clinical operations, R&D and/or medical affairs.
• Experience in radiopharmaceuticals preferred.
• Experience/expertise in interpretation of scientific data, market research, and competitive intelligence tools. Proficient in Microsoft Office Suite.
• Proven leadership skills in a cross-functional global team environment.
• Ability to interact externally and internally to support overall Company business strategy.
• Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
• Track record of success in building, developing, and managing high-performing field-based teams.
• Excellent communication skills: verbal, written and presentations.
• Demonstrated ability to develop medical affairs strategies and tactical plans.
• Detailed knowledge of regulations and compliance practices related to industry interactions with healthcare professionals.
• Proven track record of delivering results that meet or exceed targeted objectives.
• Valid driver’s license
• Ability for 75% travel