Senior Registry Manager

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🕒 Maio 22

🍂 Massachusetts – Remoto

🍂 Massachusetts – Remote

⏰ Tempo Integral

🟠 Sênior

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Thermo Fisher Scientific

SiteLinkedInTodas as Vagas

10.000+ funcionários

Fundada em 1956

🧬 Biotecnologia

💊 Farmacêutico

🔬 Ciência

Biotechnology • Pharmaceuticals • Science

A Thermo Fisher Scientific é a líder mundial em servir à ciência, com receita anual de mais de US$ 40 bilhões. Sua missão é capacitar os clientes a tornar o mundo mais saudável, limpo e seguro, apoiando a pesquisa em ciências da vida, solucionando desafios analíticos complexos, aumentando a produtividade dos laboratórios e melhorando a saúde dos pacientes por meio de diagnósticos e do desenvolvimento de terapias que transformam vidas. Com uma equipe global, oferece tecnologias inovadoras e serviços farmacêuticos por meio de marcas como Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon e PPD.

Descrição

• Responsible for full oversight and management of day-to-day activities within the entire registry • Utilize key metrics on execution and performance in its entirety • Direct and oversee assigned registry and registry team • Maintain strong relationships with participating sites • Enforce appropriate execution of IRB approved protocol, ensure full regulatory compliance is followed with each site • Ensure and monitor data queries within assigned registries are resolved in a timely manner • Strategize new business development in expansion of participating providers, sites and or registries • Organize workflow to accomplish established objectives; delegating responsibilities; training, mentoring, and evaluating team member development • Submit by the 1st of each month key performance indicators of sites participation and enrollment for assigned registry to the Director of Registry Mgt • Work alongside key CorEvitas departments to build out strategies that increase provider and subscriber participation in existing registries and create new opportunities in additional therapeutic areas • Participate in all interactions with current subscribers to appropriately communicate status of enrollment per subscriber agreement • Drive and lead input to desired changes as related to the CorEvitas Registry protocol, questionnaires, site performance metrics and assessments and EDC systems • Work alongside key leadership to balance resource allocation against achievement of company goals • Design and implement recruitment strategies for sites and investigators; work with principal investigators to overcome enrollment barriers and suggest best practices

🎯 Requisitos

• Master’s degree, preferably in life sciences, public health, health services research or related area or bachelor’s degree and equivalent experience • 6 + years’ experience in a clinical research setting • Requires GCP and HSP training certificates per policies and procedures • Experience analyzing and interpreting written material and quantitative data to draw conclusions and make recommendations based on that data • Demonstrated proficiency in accessing information stored in large data systems • Demonstrated experience using computer applications, including Microsoft Word, Excel spreadsheet and PowerPoint presentation programs, REDCap, Zelta, Salesforce

🏖️ Benefícios

• A choice of national medical and dental plans, and a national vision plan, including health incentive programs • Employee assistance and family support programs, including commuter benefits and tuition reimbursement • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount