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Senior Director, Qualitative Data Collection and Analysis

Remote in Remote, NC, US • Posted 15 hours ago • Updated 6 hours ago

Full Time

On-site

Fitment

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Job Details

Skills

Health Care
Product Launch
Science
Epidemiology
Psychology
Economics
Focus Groups
Regulatory Compliance
AIM
Business Plans
Interviewing
Professional Development
Performance Management
Thought Leadership
Data Management
Data Analysis
PCR
Data Collection
Artificial Intelligence
Management
Qualitative Research
Leadership
Research
Google Cloud Platform
Google Cloud
Budget
Forecasting
Attention To Detail
Communication
Staff Management
Cross-functional Team
Fluency
English
Innovation
Collaboration

Health Care
Product Launch
Science
Epidemiology
Psychology
Economics
Focus Groups
Regulatory Compliance
AIM
Business Plans
Interviewing
Professional Development
Performance Management
Thought Leadership
Data Management
Data Analysis
PCR
Data Collection
Artificial Intelligence
Management
Qualitative Research
Leadership
Research
Google Cloud Platform
Google Cloud
Budget
Forecasting
Attention To Detail
Communication
Staff Management
Cross-functional Team
Fluency
English
Innovation
Collaboration

Summary

Work Schedule
First Shift (Days)

Environmental Conditions
Office

Job Description

Thermo 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 management
Drive thought leadership to ensure continuous scientific improvement
Support 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 proposals
Oversee the delivery of qualitative components of PCR studies, including qualitative data collection (incl., moderation), data management, and data analysis
Collaborate with external and internal vendors that support PCR with dedicated qualitative research services
Manage 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 processes

Education 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 outputs

Knowledge, Skills, and Abilities:

Deep and demonstrated understanding of patient centered research, including a demonstrated knowledge of Google Cloud Platform 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 detail
Proven ability to lead a team to deliver high quality scientific deliverables
Demonstrated ability to delegate effectively
Strong interpersonal, organizational, communication and staff management skills and experience required
Ability to work in a cross functional team
Ability 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 sentences
Tact and sensitivity in matters relating to confidential material.
Fluency in written and oral English

Why 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.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: recfeed
Position Id: R-01361048
Posted 15 hours ago

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