Senior Clinical Research Associate

April 3

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UBC

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UBC is a company dedicated to improving patient outcomes by uniting evidence and access to specialty therapies. They offer modern, customized solutions that facilitate patient access, safety, and integrated evidence generation across various therapeutic areas, including oncology and rare diseases. With expertise in risk management, patient support, and data analytics, UBC helps biopharmaceutical companies navigate the complexities of product development and demonstrate the value of medications in real-world settings.

Evidence Development • Modernized Study Design & Execution • Late-Stage Research • Risk Evaluation & Mitigation Strategies • Pharmacovigilance

1001 - 5000 employees

Founded 2003

🧬 Biotechnology

⚕️ Healthcare Insurance

💊 Pharmaceuticals

📋 Description

• As a pharmaceutical support industry leader , UBC is devoted to empowering health solutions for a better tomorrow. • Grow your career while making a meaningful impact on the world around you. • Specific job duties: Thorough knowledge and application of project specific protocol. • Consistently completes on site monitoring in accordance with project specific timelines. • Consistently completes travel scheduling in accordance with project specific and UBC guidelines. • Responsible for content of these meetings. • Ensures follow-up of site issues and action items per UBC/sponsor timelines. • Consistently submits expense reports within UBC timelines; consistently follows UBC Travel Guidelines. • Assists management team by mentoring other Clinical Research Associates. • Assists with preparation and/or delivery of presentations for UBC Clinical Research Associate training, departmental training and/or sponsor specific training.

🎯 Requirements

• Bachelor’s degree – Life Science preferred or equivalent years of industry and monitoring experience • Minimum of 5 years experience in current role and / or related function • Minimum of 1 years experience at a Service Provider • Minimum of 3 years experience in Oncology trials and 1 year experience in Ophthalmology • Phase 1 experience required; solid tumor experience preferred • Thorough knowledge of medical terminology • Good written and verbal communication skills • Consistently meets or exceeds metrics for quality trip reports and letters • Consistently meets or exceeds metrics for completion of UBC and/or sponsor training with appropriate documentation • Ability to perform tasks in UBC’s Clinical Trial Management System, Electronic Data Capture System, Outlook and client specific systems (if applicable) • Thorough knowledge of International Conference on Harmonisaton, Good Clinical Practice guidelines, Code of Federal Regulations and UBC SOPs

🏖️ Benefits

• UBC fosters a culture built on our Core Values • We are committed to a diverse, equitable and inclusive culture