Senior Site Activation Manager

🕒 Setembro 7

🌲 North Carolina – Remoto

🌲 North Carolina – Remote

💵 $107.000 - $213.000 / ano

⏰ Tempo Integral

🟠 Sênior

👔 Gerente

🦅 Patrocina Visto H1B

Esta empresa já patrocinou vistos H1B no passado.

👻 Score fantasma 11%

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 66 dias.
• As vagas desta empresa costumam ser preenchidas em 34 dias.

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Worldwide Clinical Trials

SiteLinkedInTodas as Vagas

1001 - 5000 funcionários

🏥 Saúde

💼 Consultoria

📦 Logística

Healthcare • Consulting • Logistics

Worldwide Clinical Trials é uma organização global de pesquisa clínica por contrato (CRO) que oferece serviços abrangentes de ensaios clínicos. A empresa é especializada em apoiar estudos em diversas áreas terapêuticas, como oncologia, cardiologia e doenças raras. Com mais de 30 anos de experiência, a Worldwide Clinical Trials enfatiza suporte personalizado e soluções sob medida ao longo de todo o ciclo de vida do desenvolvimento de medicamentos. Seus serviços incluem monitoramento clínico, gestão de dados, recrutamento de pacientes e consultoria regulatória, garantindo precisão e atenção personalizada para cada ensaio clínico.

Descrição

• Serve as the primary point of communication and accountability for study start-up and maintenance activities on assigned projects • Oversee project activities of functional groups involved in site activation to ensure critical path activities are completed on time and within budget • Ensure accurate compilation, management, tracking and analysis of site activation activities in a timely manner • Support feasibility and/or site identification activities, as needed • Work closely with assigned team members to expedite the Site Qualification and Selection process • Effectively communicate Site Activation & Regulatory project status to the Sponsor, GPL/CPM and project team • Coordinate, collaborate and oversee site identification and central and local ECs activities for NA countries • Progress essential document collection and monitor investigator and site contract status • Perform country- and study-specific site activation tasks in accordance with GCPs, applicable regulations, and SOPs • Provide site activation-related input into proposal text and budget items when supporting pre-award activities • Report to a senior member of the Site Activation leadership team within the assigned therapeutic area

🎯 Requisitos

• Proven leadership and organizational management skills in planning, strategizing, managing, monitoring, scheduling, and critiquing • Demonstrated ability to exercise sound judgment and consistently make decisions independently to proactively prevent and solve problems • Demonstrated ability to consistently and positively have an impact on initiatives relating to interacting with sites and/or customers • Demonstrated ability to motivate, lead and engage a team to consistently and successfully achieve meaningful goals • Demonstrated ability to perform and thrive in ambiguous situations • Strong interpersonal skills in a fast-paced, deadline oriented, and changing environment • A minimum four-year college curriculum or equivalent with a major concentration in medical, biological, physical, health, pharmacy or other related science, or two-year college degree plus four years experience within clinical research • Seven years relevant CRO/pharmaceutical industry experience, preferably in Start-up Management, Project Management, and/or Site Management experience • Proficient in cross-cultural communication • Proficient in both spoken and written English • Work location: Durham, North Carolina, United States

🏖️ Benefícios

• Competitive benefits package depending on location • Inclusive and equitable workplace • Transparent compensation and pay equity

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