Clinical Trial Associate

🔥 0 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👻 Ghost score 10%

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Perspective Therapeutics

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2023

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

💰 $400k Grant on 2024-02

Healthcare • Manufacturing • Biotechnology

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.

📋 Description

• Provide comprehensive administrative and operational support to the Clinical Operations Team • Provide general administrative support to Clinical Operations and Project Management Departments • Assist Clinical Operations teams with ongoing study conduct and required project tasks • Coordinate internal and external meetings, prepare activities, and generate meeting minutes • Facilitate outreach to potential clinical trial sites and initial site feasibility procedures • Lead quarterly documentation and compliance checks using internal trackers and the eQMS system • Act as super user for the electronic Trial Master File system and track eTMF progress • Create professional slide presentations for internal and external stakeholders • Set up, collect, register, organize, and maintain clinical study documentation • Prepare documentation for audits, final reconciliation, and archival according to GCP guidelines • Coordinate ordering, dispatch, and tracking of study materials • Organize data collection forms and other study materials, including logging, tracking, and quality control • Assist with tracking and distribution of correspondence and reports • Coordinate document translation

🎯 Requirements

• Bachelor's degree in a relevant field (life sciences, healthcare, etc.) • Research or health care-related academic or work experience preferred • Excellent computer literacy and application skills, including Microsoft Word, Excel, PowerPoint, and Outlook • Ability to become familiar with ICH-GCP, FDA, and other appropriate regulations and relevant SOPs • Strong organizational skills and ability to manage multiple tasks with meticulous attention to detail • Ability to work collaboratively in a team-oriented environment • Clear written and verbal communication skills in English • May be required to sit or stand for long periods of 8+ hours a day

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