Senior Director - Medical Monitor

February 14

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Perspective Therapeutics

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Perspective Therapeutics is a biotechnology company focused on developing innovative cancer treatments through a unique class of theranostics. Their proprietary technologies enable the targeting of specific tumors for treatment while minimizing toxicity to healthy tissues. By utilizing radiation, radiopharmaceuticals, and advanced imaging technologies, they aim to improve treatment efficacy and provide better outcomes for cancer patients.

Oncology • Cancer Treatment • Radiopharmaceuticals • Imaging Technologies & Diagnostics

51 - 200 employees

Founded 2023

🧬 Biotechnology

⚕️ Healthcare Insurance

💊 Pharmaceuticals

💰 $400k Grant on 2024-02

📋 Description

• The Senior Director, Medical Monitor will oversee medical and scientific aspects of clinical trials. • Requires deep understanding of oncology and ability to work cross-functionally. • Monitor patient safety, therapeutic efficacy, and integrity of clinical trial data. • Ensure compliance with ethical standards and regulations in clinical trials. • Serve as primary medical contact for clinical trial sites and provide mentorship. • Collaborate with teams to ensure smooth design and execution of trials. • Contribute to regulatory document development and clinical trial data analysis. • Stay current with advances in oncology and clinical research methodologies.

🎯 Requirements

• Medical Doctor (MD) degree from an accredited medical school required. • Board certification in oncology preferred. • 3-5+ years of clinical practice experience in the relevant therapeutic area, with a focus on oncology or nuclear medicine preferred. • 2+ years of industry experience in clinical development, including hands-on involvement with early to late-phase clinical trials (Phase I-IV). • Experience in the preparation and review of clinical trial documents, including protocols, informed consent forms, and regulatory submissions. • Experience in medical monitoring and ensuring the safety of study participants during clinical trials is highly desirable. • Strong knowledge of Good Clinical Practice (GCP), FDA regulations, and ICH guidelines. • Outstanding leadership, collaboration, and teamwork in a cross-functional setting; comfortable with a hands-on leadership position. • Excellent communication and interpersonal skills, with the ability to work collaboratively in a cross-functional team environment. • Strong analytical and problem-solving skills, with a keen attention to detail. • Ability to manage multiple projects simultaneously and prioritize tasks effectively. • Must be willing to travel up to 20% of the time. Both domestic and international travel may be required.