
1001 - 5000 funcionários
Fundada em 2003
🧬 Biotecnologia
⚕️ Seguro de Saúde
💊 Farmacêutico
Biotechnology • Healthcare Insurance • Pharmaceuticals
A UBC é uma empresa dedicada a melhorar os resultados dos pacientes, conectando terapias especializadas aos pacientes que delas necessitam. Eles oferecem soluções modernas e personalizadas, focando em acesso, segurança e geração de evidências para produtos biofarmacêuticos. A UBC é especializada em desenvolvimento de evidências, gestão de riscos e acesso do paciente, utilizando dados do mundo real e tecnologias inovadoras para otimizar a jornada de saúde e garantir o uso eficaz de medicamentos.
🕒 Fevereiro 19
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

1001 - 5000 funcionários
Fundada em 2003
🧬 Biotecnologia
⚕️ Seguro de Saúde
💊 Farmacêutico
Biotechnology • Healthcare Insurance • Pharmaceuticals
A UBC é uma empresa dedicada a melhorar os resultados dos pacientes, conectando terapias especializadas aos pacientes que delas necessitam. Eles oferecem soluções modernas e personalizadas, focando em acesso, segurança e geração de evidências para produtos biofarmacêuticos. A UBC é especializada em desenvolvimento de evidências, gestão de riscos e acesso do paciente, utilizando dados do mundo real e tecnologias inovadoras para otimizar a jornada de saúde e garantir o uso eficaz de medicamentos.
• Lead UBC project teams to deliver project milestones • Serve as the primary contact with the sponsor for all study related items • Oversee all aspects of project conduct • Execute operational aspects of assigned project activities • Assist in the development and design of protocols, CRFs, regulatory documents, project master file • Monitor project progress as compared to established plans • Facilitate and plan investigator meetings • Supervise APM/PMs and other team members • Provide reports to the Sponsor on project progress • Maintain project documentation to be 'audit ready' • Lead internal client teleconferences and/or meetings • Support APM/PMs in sponsor/regulatory audits
• 5 years of experience managing global clinical trials within the CRO industry • Observational study experience • Oncology experience is a plus • BA Degree or minimum 5 years of direct project management experience at a CRO • Excellent written, verbal and non-verbal communication skills • Excellent supervisory skills • Excellent interpersonal skills • Excellent presentation skills • Ability to independently assess issues and/or mitigate risk by using critical judgment • Solution driven • Manage competing priorities effectively • Very good knowledge of regulatory requirements (i.e. Good Clinical Practice, ICH guidelines, etc.)
• 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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