Job Description

As a Senior Research Consultant on diverse projects, you will play a critical role in leading evidence synthesis projects. Collaborating closely with Cytel's leadership team, you will have the opportunity to deliver exceptional services conducting litrerature reviews using Cytel's cutting-edge products including LiveSLR and LiveNMA.




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Join Cytel as a Senior Research Consultant and be part of a company driving innovation within Health Economics and Outcomes Research (HEOR)

Education, Professional Skills & Experience:

Advanced degree in life sciences, health economics, or a clinical discipline is preferred (e.g., PhD, PharmD, MPH, MS). 3 to 5 years of experience in conducting SLRs, and 5-8 years within the field of health economics and outcomes research (HEOR) and/or consultancy. Proficiency in English, including reading, writing, and oral communication. Ability to absorb and synthesize a broad range of information, including clinical and scientific data. Working knowledge of pharmaceutical product development and HEOR. Methodological, disciplined, well-organized, and professional approach. Strong ability to work independently and as part of a team. Excellent attention to detail and efficiency in managing large databases of studies and data extraction. Strong multitasking and prioritization skills. Advanced Microsoft Office skills to present information in an engaging, clean, and concise manner.
Join our team at Cytel, a dynamic and innovative company that values scientific excellence, collaboration, and personal growth. As a Senior Research Consultant, you will have the opportunity to make a meaningful impact on evidence synthesis while working with cutting-edge SLR software products. We offer a supportive work environment that encourages innovation and professional development.



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Education, Professional Skills & Experience:

Advanced degree in life sciences, health economics, or a clinical discipline is preferred (e.g., PhD, PharmD, MPH, MS). 3 to 5 years of experience in conducting SLRs, and 5-8 years within the field of health economics and outcomes research (HEOR) and/or consultancy. Proficiency in English, including reading, writing, and oral communication. Ability to absorb and synthesize a broad range of information, including clinical and scientific data. Working knowledge of pharmaceutical product development and HEOR. Methodological, disciplined, well-organized, and professional approach. Strong ability to work independently and as part of a team. Excellent attention to detail and efficiency in managing large databases of studies and data extraction. Strong multitasking and prioritization skills. Advanced Microsoft Office skills to present information in an engaging, clean, and concise manner.
Join our team at Cytel, a dynamic and innovative company that values scientific excellence, collaboration, and personal growth. As a Senior Research Consultant, you will have the opportunity to make a meaningful impact on evidence synthesis while working with cutting-edge SLR software products. We offer a supportive work environment that encourages innovation and professional development.



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Key Responsibilities

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Develop and execute SLR protocols for clinical efficacy and effectiveness, health-related quality of life (HRQoL), healthcare resource use (HCRU), costs, and economic evaluations. Perform quality checks on screening, data extraction, risk of bias and data upload into our LiveSLR software. Can develop search strategies and i nterpret and summarize evidence, providing insights and updates to internal and external stakeholders. Has been involved in HTA submissions and is knowledgeable of EU-JCA guidelines Manage internal and external project plans, ensuring timely delivery and effective communication. Whilst respecting QC process, can be independent for his/her projects most of the time Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors Demonstrates good judgment in selecting methods and techniques for obtaining solutions Can be involved in multiple projects (e.g. up to 5-6 mid-size projects) and can be project lead in a workstream Communicate actively 100% - resolves issues by proposing solutions Networks with senior internal and external colleagues in area of expertise Take ownership of deliverables (internally and with clients), including client communications (e.g. emails, slide presentations) Can teach / transfer knowledge around core tasks Actively support BD activities including proposal writing, scoping w clients Understands the operational management of a project ExternalResponsibilitiesStr

Key Responsibilities

:


Develop and execute SLR protocols for clinical efficacy and effectiveness, health-related quality of life (HRQoL), healthcare resource use (HCRU), costs, and economic evaluations. Perform quality checks on screening, data extraction, risk of bias and data upload into our LiveSLR software. Can develop search strategies and i nterpret and summarize evidence, providing insights and updates to internal and external stakeholders. Has been involved in HTA submissions and is knowledgeable of EU-JCA guidelines Manage internal and external project plans, ensuring timely delivery and effective communication. Whilst respecting QC process, can be independent for his/her projects most of the time Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors Demonstrates good judgment in selecting methods and techniques for obtaining solutions Can be involved in multiple projects (e.g. up to 5-6 mid-size projects) and can be project lead in a workstream Communicate actively 100% - resolves issues by proposing solutions Networks with senior internal and external colleagues in area of expertise Take ownership of deliverables (internally and with clients), including client communications (e.g. emails, slide presentations) Can teach / transfer knowledge around core tasks Actively support BD activities including proposal writing, scoping w clients * Understands the operational management of a project