
1001 - 5000 employees
Founded 2003
🏥 Healthcare
💼 Consulting
🧬 Biotechnology
Healthcare • Consulting • Biotechnology
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.
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1001 - 5000 employees
Founded 2003
🏥 Healthcare
💼 Consulting
🧬 Biotechnology
Healthcare • Consulting • Biotechnology
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.
• Write risk management documents • Manage operations of assigned risk management projects, epidemiologic studies, and/or registries • Serve as scientific lead for risk management projects • Participate in epidemiology, registry, and risk management-related projects • Contribute to the preparation, design, and writing of REMS, KAB protocols and surveys, reports, abstracts, and other related documents • Collaborate with physicians, epidemiologists, clients, and internal UBC groups • Participate in internal and client project teams and meetings • Develop observational program protocols • Coordinate project activities and track projects, timelines, tasks, and deliverables • Serve as client point of contact • Provide input to Contracts Management for scope-of-work and budget revisions • Communicate project deliverables and milestones to Finance for invoicing tracking • Develop project timelines, schedule meetings, and prepare meeting minutes • Support proposal development, including service descriptions and budgets • Attend client, bid defense, and industry meetings; present at industry meetings when appropriate
• 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 is helpful • Strong written and verbal communication/interpersonal skills • Ability to work independently and 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, detail-oriented, self-motivated, and quality driven • Strong computer skills, including word processing and proficiency with tables and figures • Ability to work after business hours and on weekends as necessary to meet critical deadlines
• Remote opportunities • Competitive salaries • Growth opportunities for promotion • 401K with company match • Tuition reimbursement • Flexible work environment • Discretionary 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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