Clinical Research Project Manager – PST/EST/CST Timezone

Vaga não está no LinkedIn

🕒 4 dias atrás

🇲🇽 México – Remoto

⏰ Tempo Integral

🟡 Pleno

🟠 Sênior

🧪 Pesquisa Clínica

👻 Score fantasma 25%

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.Como pontuamos: tempo em aberto, republicações, vagas abertas vs tamanho do time, rapidez para fechar vagas, e se o salário está divulgado.Observação: é uma estimativa de dados públicos, não um julgamento da empresa. Vagas reais podem ter pontuação alta, então use como uma dica, não como um fato.

Candidatar-se

Encontrar Vagas Remotas Similares

UniTriTeam

SiteLinkedInTodas as Vagas

11 - 50 funcionários

Fundada em 2021

🏥 Saúde

🤝 B2B

🎯 Recrutamento

Healthcare • B2B • Recruitment

A UniTriTeam é uma empresa de serviços de saúde que ajuda organizações de saúde e pesquisa clínica a escalarem suas operações de forma eficiente e em conformidade. A empresa oferece suporte à pesquisa clínica e serviços de operações, incluindo aumento de equipe global, design e manutenção de estudos eSource, entrada de dados em EDC, serviços de e-regulatório, recrutamento de pacientes, administração e integração de CTMS, inteligência de negócios e análise de dados, além de suporte financeiro/contábil. Também oferece serviços de tecnologia (CTMS, Salesforce, Monday. com, HubSpot, SharePoint, NetSuite) e soluções de aquisição de talentos, como recrutamento e serviços de colocação internos.

Descrição

• Own and manage the study start-up process from initial study award or feasibility through site activation and readiness for first patient enrollment • Develop study start-up plans, timelines, milestones, and deliverables • Coordinate regulatory, contracts, budgets, clinical operations, finance, recruitment, technology, and other functional teams • Track feasibility, regulatory submissions, IRB approvals, contracts, budgets, training, system readiness, and sponsor requirements • Ensure documentation, approvals, and operational requirements are completed before site activation • Identify critical-path activities, dependencies, and potential delays; implement mitigation plans • Drive timely completion of start-up milestones while maintaining compliance and quality standards • Serve as the central coordination point across internal departments, sponsors, CROs, vendors, and site leadership • Lead study start-up meetings, assign action-item owners, and ensure follow-through • Communicate responsibilities, deadlines, expectations, study progress, priorities, risks, and milestones • Escalate risks, delays, and unresolved issues with recommended solutions and recovery plans • Build and maintain project plans, study start-up trackers, centralized documentation, and status reports • Monitor milestones, deliverables, readiness, competing priorities, bottlenecks, and project schedules • Coordinate operational readiness including staffing, training, supplies, systems, and documentation • Verify readiness of CTMS, eRegulatory, eSource, EDC, and other study-specific systems • Ensure alignment with GCP, regulatory requirements, sponsor expectations, and organizational SOPs • Support handoffs from study start-up to ongoing clinical research operations • Improve workflows, handoffs, standardized processes, and study activation timelines • Facilitate productive meetings with documented decisions, owners, and due dates • Serve as a trusted partner to client leadership • Achieve on-time study activation, milestone adherence, deliverable completion, risk resolution, project visibility, cross-functional effectiveness, and continuous improvement

🎯 Requisitos

• Bachelor's degree in life sciences, healthcare administration, clinical research, or a related field; equivalent relevant experience may be considered • Minimum 3–5 years of experience in clinical research, preferably within clinical trial operations, site operations, or study start-up • Demonstrated experience managing clinical research projects, study start-up activities, or site activation processes • Strong understanding of the clinical trial lifecycle, particularly feasibility, regulatory requirements, IRB submissions, contracts, budgets, and site activation • Experience coordinating multiple functional departments and managing interdependent deliverables • Strong knowledge of Good Clinical Practice (GCP), clinical research regulations, and standard operating procedures • Proficiency with project management tools, trackers, Microsoft Excel, and collaborative platforms • Exceptional written and verbal communication skills • Demonstrated ability to manage multiple studies or projects simultaneously while maintaining accuracy and meeting deadlines • Experience working within a clinical research site, site network, SMO, CRO, or sponsor organization • Direct experience managing multiple study activations concurrently • Familiarity with CTMS, eRegulatory, eSource, and EDC platforms such as CRIO, Clinical Conductor, RealTime, Florence, or comparable systems • Experience developing study start-up dashboards, standardized trackers, and operational performance reports • PMP, ACRP, SOCRA, or other relevant professional certification • Experience improving clinical research workflows and reducing study start-up cycle times • Strong organizational, detail-oriented, proactive, self-directed, accountable, results-driven, cross-functional leadership, and fast-paced execution abilities

🏖️ Benefícios

• Full-time employment • Remote work arrangement • Client-specific remote requirements • Opportunity to work with clinical research organizations • Professional involvement in operational, regulatory, technology, and project management support • Opportunities to improve efficiency, strengthen execution, and scale clinical research operations

📊 Verifique sua pontuação de currículo para esta vaga

Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

Enviar Currículo