UBC is a company dedicated to improving patient outcomes by connecting specialty therapies to patients in need. They provide modern and customized solutions focusing on access, safety, and evidence generation for biopharmaceutical products. UBC specializes in evidence development, risk management, and patient access, utilizing real-world data and innovative technologies to optimize the healthcare journey and ensure effective medication use.
Evidence Development • Modernized Study Design & Execution • Late-Stage Research • Risk Evaluation & Mitigation Strategies • Pharmacovigilance
March 27
UBC is a company dedicated to improving patient outcomes by connecting specialty therapies to patients in need. They provide modern and customized solutions focusing on access, safety, and evidence generation for biopharmaceutical products. UBC specializes in evidence development, risk management, and patient access, utilizing real-world data and innovative technologies to optimize the healthcare journey and ensure effective medication use.
Evidence Development • Modernized Study Design & Execution • Late-Stage Research • Risk Evaluation & Mitigation Strategies • Pharmacovigilance
• Responsible for writing risk management documents • Managing the operation of assigned risk management projects • Interfacing with the client and collaborating with the scientific leaderships as well as internal UBC groups • Coordinate project-related activities with the client and serve as point of contact • Provide input to Contracts Management group to revise scope of work as needed for projects and budget revisions as required • Develop project timelines, schedule project meetings, and develop meeting minutes • Support development of proposals – both description of services and budget • Attend client meetings as needed including bid defense meetings as well as relevant industry meetings
• Bachelor’s degree in life sciences, healthcare, and/or public health or equivalent • Experience in protocol writing, study design and operations is helpful • Familiarity with clinical trials, drug development and medical and scientific terminology • Strong written and verbal communication/ interpersonal skills • Ability to work independently, yet function well in a small team environment • Ability to prioritize and work on multiple projects simultaneously • Knowledge of project management techniques and tools • Professional, organized, detailed-oriented with a high degree of accuracy, self-motivated and quality driven • Enjoys fast-paced environment, challenge of learning about different health-related and research areas • Strong computer skills (word processing, including proficiency with tables and figures)
• Remote opportunities • Competitive salaries • Growth opportunities for promotion • 401K with company match* • Tuition reimbursement • Flexible work environment • Discretionary PTO (Paid Time Off) • Paid Holidays • Employee assistance programs • Medical, Dental, and vision coverage • HSA/FSA • Telemedicine (Virtual doctor appointments) • Wellness program • Adoption assistance • Short term disability • Long term disability • Life insurance • Discount programs
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