Project Manager II – Virology Phase 1

🕒 Abril 15

🏄 California – Remoto

🏄 California – Remote

⏰ Tempo Integral

🟡 Pleno

🟠 Sênior

👷‍♀️ Gerente de Projetos

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Syneos Health

SiteLinkedInTodas as Vagas

10.000+ funcionários

🧬 Biotecnologia

💊 Farmacêutico

⚕️ Seguro de Saúde

Biotechnology • Pharmaceuticals • Healthcare Insurance

Syneos Health é uma organização líder, totalmente integrada, de soluções biofarmacêuticas, criada para acelerar o sucesso dos clientes. A empresa transforma insights exclusivos clínicos, de Assuntos Médicos (Medical Affairs) e comerciais em resultados para responder às realidades modernas do mercado. Ao utilizar tecnologias avançadas e insights, a Syneos Health colabora com os clientes para acelerar a entrega de terapias importantes a pacientes no mundo todo, oferecendo serviços que abrangem todo o espectro do clínico ao comercial.

Descrição

• Plan, direct, create, and communicate clinical study timelines to ensure deliverables are produced on schedule • Gather input from cross-functional teams to create comprehensive plans for clinical studies • Ensure consistency of clinical study processes across clinical trials, adhering to standard operating procedures (SOP), good clinical practice (GCP), and specific country regulations • Oversee and resolve operational aspects of clinical trials in conjunction with project teams • Select sites and vendors, prepare clinical trial budgets, and ensure studies are conducted within clinical trial protocols • Monitor progress and follow up with team members and line managers when issues develop • Implement and prepare the clinical development strategy as outlined by the clinical teams • Develop trial recruitment strategies to ensure successful participant enrollment

🎯 Requisitos

• Bachelor's degree in a related field (e.g., Clinical Research, Life Sciences, Healthcare Management) • Minimum of 5 years of experience in clinical project management or a related role • Proven track record of successfully managing clinical trials and ensuring adherence to SOP, GCP, and country regulations • Certification in Clinical Research (e.g., CCRP, CCRA) is preferred • Project Management Professional (PMP) certification is a plus • Strong organizational and planning skills to create and manage clinical study timelines • Excellent communication skills to gather input from cross-functional teams and communicate plans effectively • Ability to oversee and resolve operational aspects of clinical trials • Knowledge of SOP, GCP, and country regulations to ensure consistency across clinical studies • Experience in site and vendor selection, budget preparation, and monitoring progress • Ability to implement and prepare clinical development strategies • Strong problem-solving skills to address issues that arise during clinical trials

🏖️ Benefícios

• Company car or car allowance • Health benefits to include Medical, Dental and Vision • Company match 401k • Eligibility to participate in Employee Stock Purchase Plan • Eligibility to earn commissions/bonus based on company and individual performance • Flexible paid time off (PTO) and sick time