UBC
UBC is a specialized biopharmaceutical solutions company that connects specialty therapies to patients in need. They focus on enhancing patient outcomes by providing customized solutions in access, safety, and evidence generation. UBC employs innovative strategies to facilitate patient access to therapies and generate valuable evidence for stakeholders, ensuring the effective and safe use of medications throughout their lifecycle.
Evidence Development • Modernized Study Design & Execution • Late-Stage Research • Risk Evaluation & Mitigation Strategies • Pharmacovigilance
Senior Clinical Research Associate
April 4
UBC
UBC is a specialized biopharmaceutical solutions company that connects specialty therapies to patients in need. They focus on enhancing patient outcomes by providing customized solutions in access, safety, and evidence generation. UBC employs innovative strategies to facilitate patient access to therapies and generate valuable evidence for stakeholders, ensuring the effective and safe use of medications throughout their lifecycle.
Evidence Development • Modernized Study Design & Execution • Late-Stage Research • Risk Evaluation & Mitigation Strategies • Pharmacovigilance
📋 Description
• As a pharmaceutical support industry leader, UBC is devoted to empowering health solutions for a better tomorrow. • We provide services to enhance the entire drug development process and commercialization lifecycle. • Specific job duties include monitoring site compliance with protocols, maintaining contact with sites, and managing the documentation process. • UBC fosters a culture built on our Core Values of Collaboration, Conscientiousness, Curiosity, Compassion and Consultation.
🎯 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 year 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 • Ability to perform tasks in UBC’s Clinical Trial Management System • Thorough knowledge of International Conference on Harmonisation, Good Clinical Practice guidelines, Code of Federal Regulations and UBC SOPs
🏖️ Benefits
• Equal opportunity employer • Inclusive workplace • Opportunities for career growth • Commitment to improving patient outcomes
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