
10.000+ funcionários
🏥 Saúde
💼 Consultoria
📦 Logística
Healthcare • Consulting • Logistics
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.
🕒 Outubro 8
🗣️🇺🇸🇬🇧 Inglês obrigatório
De onde vem esta vaga
Publicada na página de carreiras da Syneos Health, não em um site de vagas
Vista pela primeira vez pelo Remote Rocketship Outubro 8
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

10.000+ funcionários
🏥 Saúde
💼 Consultoria
📦 Logística
Healthcare • Consulting • Logistics
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.
• Provide site management oversight, clinical monitoring and central monitoring deliverables, focusing on patient safety, protocol/GCP/regulatory compliance and data integrity • Oversee site interactions from activation through closeout, including recruitment, investigator payments and related activities • Identify critical data, process and protocol-execution risks and develop mitigations using the RACT • Review study scope, budget and protocol content and ensure clinical project teams understand contractual obligations • Identify and escalate risks to timelines, quality, budget and contracted scope • Participate in and present at key meetings, including Kick Off Meetings • Serve as an escalation point for investigator site staff communications and interact with investigators and site staff by phone or in person • Collaborate with Study Start Up, Patient Recruitment, Data Management and other functions to meet study milestones • Develop and maintain clinical study tools and templates, including Clinical Monitoring Plans • Ensure CTMS, dashboards and other systems are configured and available, including user acceptance testing and access/audit trail reviews • Coordinate study-team training on protocols, CRF completion, dashboards, SOPs, clinical plans, data plans and timelines • Oversee CRA and Central Monitor resourcing, site assignments and study-team conduct • Ensure quality and visibility of clinical monitoring, central monitoring and site management deliverables • Review oversight dashboards and clinical trial systems including CTMS, EDC, eDiary, ePRO, TMF, IVRS/IWRS and central monitoring dashboards • Oversee compliance with monitoring strategies, CMP/SMP and risk plans • Review site and central monitoring documentation and ensure timely, compliant delivery • Provide client, project management and leadership updates on deliverables and risks • Support inspection readiness, corrective action plans, data cuts and database lock deadlines • Oversee CRAs and Central Monitors, assess compliance and identify emerging risks • Provide staff-performance feedback to line managers; may support larger, more complex trials
• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience • Demonstrated ability to lead and align teams in the achievement of project milestones • Demonstrated capability of working in an international environment • Demonstrated expertise in site management and monitoring (clinical or central) • Preferred experience with risk-based monitoring • Understanding of clinical trial management financial principles and budget management • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements • Good computer skills • Good communication, presentation and interpersonal skills among project team and with sites • Strong conflict resolution skills • Ability to apply problem-solving techniques to resolve complex issues and apply a risk management approach • Critical thinking to determine causes and appropriate solutions to issues • Moderate travel may be required, approximately 20%
• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Total Self culture supporting authenticity and inclusion • Diversity, equity and belonging initiatives
Candidatar-se🕒 Outubro 6
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🗣️🇺🇸🇬🇧 Inglês obrigatório
🕒 Outubro 2
Gerente Sênior de Ensaios Clínicos responsável pela entrega de ensaios clínicos na ICON, uma organização global de inteligência em saúde e pesquisa clínica. Gerenciamento de orçamentos, recrutamento de participantes, supervisão de estudos e equipes multifuncionais.
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🕒 Setembro 17
Clinical Trial Coordinator supporting pharmaceutical and biotech clinical trials. Managing documentation, regulatory tracking, systems, and study operations remotely in Mexico.
🗣️🇺🇸🇬🇧 Inglês obrigatório
🕒 Julho 27
Remote Clinical Research Coordinator supporting clinical trial operations and patient outreach in clinical research. Working with global teams in a fully remote role across multiple time zones.
🇲🇽 México – Remoto
💰 $5.000.000 Series A - Indeed em 2005-07
⏰ Tempo Integral
🟢 Júnior
🟡 Pleno
🧪 Pesquisa Clínica
🗣️🇺🇸🇬🇧 Inglês obrigatório