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Senior Director, Qualitative Data Collection and Analysis
200510503Z Thermo Fisher Scientific Pte. Ltd.
11h ago
0ManagementUnited Stateshimalayas
Qualitative-ResearchResearch-LeadershipPatient-Centered-ResearchHealthcare-ResearchClinical-Outcomes-AssessmentSenior-Director-ResearchDirector-Of-Data-&-InsightsSenior-Director-AnalystDirector
Job Description
Work ScheduleFirst Shift (Days)Environmental ConditionsOfficeJob DescriptionThermo Fisher Scientific’s Patient-Centered Research (PCR) group helps sponsors to integrate the patient voice in all relevant healthcare decisions, from development over regulatory to reimbursement and product launch. For that, PCR uses a unique combination of scientific fields, including health sciences, psychometrics, epidemiology, psychology, health economics and others. Our work has helped identify and clarify unmet clinical needs, assess burden of illness and evaluate patient outcomes, preference and/or adherence, while supporting promotional and labeling claims on a global scale.The Senior Director of Qualitative Data Collection and Analysis (QDA) is primarily responsible for the collection, organization and analysis of qualitative data on PCR projects, including: moderation of interviews and focus groups, management of vendors for dedicated qualitative research services, oversight of qualitative research technologies (incl., AI-enabled solutions), and qualitative data analysis. As part of this remit the Senior Director will be responsible for leading the development, improvement and implementation of quality and compliance assurance processes. The aim of this exciting role is to build a best-in-class qualitative research center of excellence that supports our scientific solution teams with its methodological expertise.This role is critical for our mission to provide a full suite of services and offerings to achieve patient focused drug development.What You’ll Do:Develop and implement annual QDA business plans, including identifying and implementing a best-in-class qualitative delivery model.Monitor industry developments to ensure the team has access to best-in-class capabilities. Collaborate with all PCR solution teams (i.e., clinical outcomes assessment, in-trial research, patient preferences, real-world experience and insights) to ensure the successful design and delivery of projects.Manage staff, including interviewing and selection, job description preparation, professional development, goal setting, performance management and any other tasks associated with staff functions and managementDrive thought leadership to ensure continuous scientific improvementSupport opportunity management to optimize win rates, including leading the development of qualitative research strategies to meet client needs, and ensuring these are appropriately represented in proposalsOversee the delivery of qualitative components of PCR studies, including qualitative data collection (incl., moderation), data management, and data analysisCollaborate with external and internal vendors that support PCR with dedicated qualitative research servicesManage qualitative research technologies for data collection and analysis (incl., AI enablement)Work with relevant internal stakeholders to develop, manage, improve and implement qualitative research standards and processesEducation and Experience:PhD, Master’s or Bachelor’s (PhD preferred)At least 12 years of qualitative research leadership in a relevant field with a track record of scientific outputsKnowledge, Skills,and Abilities:Deep and demonstrated understanding of patient centered research, including a demonstrated knowledge of GCP and awareness of working in a regulatory environment.Ability to develop business strategies and plans.Understanding of budgeting and forecasting with the ability to interpret data with attention to detailProven ability to lead a team to deliver high quality scientific deliverablesDemonstrated ability to delegate effectivelyStrong interpersonal, organizational, communication and staff management skills and experience requiredAbility to work in a cross functional teamAbility to communicate complex information and ideas so that others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentencesTact and sensitivity in matters relating to confidential material.Fluency in written and oral EnglishWhy Join Us?When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthrough.Originally posted on Himalayas
