Clinical Project Research Manager – EDS, RWE, NIS

🕒 Outubro 23

🇺🇸 Estados Unidos – Remoto (EUA)

⏰ Tempo Integral

🟡 Pleno

🟠 Sênior

👔 Gerente

👻 Score fantasma 10%

O que significa: a chance de ninguém estar realmente contratando para esta vaga.Como ler: 60% ou mais significa que achamos que é uma vaga fantasma. Pontuações mais baixas preocupam menos.Por que essa pontuação:

• Aberta há 19 dias.
• As vagas desta empresa costumam ser preenchidas em 22 dias.
• Sem salário divulgado.

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UBC

SiteLinkedInTodas as Vagas

1001 - 5000 funcionários

Fundada em 2003

🏥 Saúde

💼 Consultoria

🧬 Biotecnologia

Healthcare • Consulting • Biotechnology

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.

Descrição

• Plan, organize, and lead UBC project teams to deliver projects based on client needs on time, on budget, and within scope • Oversee all aspects of project conduct from start-up through close-out • Execute operational aspects of assigned project activities and special projects • Manage projects according to scope of work and contracted budget • Manage project revenue and invoicing • Ensure projects follow UBC and applicable client SOPs • Develop and monitor project plans and processes for contracted milestones • Prepare project timelines and coordinate deliverables • Prepare meeting agendas and create minutes and action logs • Track project budgets against contract milestones • Serve as primary UBC contact with sponsors • Coordinate and facilitate internal and external project meetings • Resolve project team member questions • Supervise cross-functional project support areas • Ensure project training and assist with training • Develop content and lead internal and external kickoff meetings • Negotiate budgets and assist with contract remediation • Present project information at bid defenses, client meetings, and monthly project reviews • Maintain audit-ready project documentation • Participate in sponsor/regulatory audits • Coordinate investigator meetings • Assist with protocol development and patient/subject consent forms or REMS documents as required • Lead process improvement activities • Establish, implement, and track project metrics • Coordinate and maintain the Trial Master File • Perform CSS and CRA duties as needed • Perform other duties assigned by management • Supervise the project team

🎯 Requisitos

• Bachelor’s Degree or equivalent experience • Previous managerial, or relevant experience, required • Excellent written verbal and non-verbal communication skills • Excellent supervisory, interpersonal, and presentation skills • Ability to independently assess issues and/or mitigate risk by using critical judgment to come to a resolution • Solution driven • Knowledge of regulatory requirements (i.e. Good Clinical Practice, ICH guidelines, etc.) • 10% travel as required

🏖️ Benefícios

• 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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