Research Associate III – Clinical Outcomes Assessment

🔥 34 minutes ago

🌐 Netherlands, Denmark, +7 more countries – Remote

🇳🇱 Netherlands – Remote 🇩🇰 Denmark – Remote 🇫🇷 France – Remote 🇭🇺 Hungary – Remote 🇸🇪 Sweden – Remote 🇮🇹 Italy – Remote 🇵🇱 Poland – Remote 🇬🇧 United Kingdom – Remote 🇪🇸 Spain – Remote

⏰ Full Time

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Support the Principal Investigator in developing study designs, budgets, and proposals, including outcome selection, sample size, and analysis approach • Develop protocols, analysis plans, technical reports, and other deliverables for PI and client review • Coordinate and support junior staff throughout projects • Communicate with and manage internal and external stakeholders and vendors, including patient advocacy groups and other departments • Conduct qualitative interview studies and/or surveys with patients, caregivers, and investigators • Contribute to quantitative study approaches, including response options, scoring, and planned analyses • Support development, testing, and validation of fit-for-purpose clinical outcome assessments • Evaluate measurement properties including reliability, validity, responsiveness, and meaningful change • Manage qualitative and quantitative data analysis and quality control, including descriptive and inferential analyses • Review analysis outputs and interpret findings • Contribute to manuscripts, posters, and oral presentations at conferences • Contribute to wider Patient-Centered Research team projects • Track project timelines and budget use with the Project Management Office • Maintain electronic filing, SOP, and IRB compliance • Stay current with relevant research and contribute to PCR initiatives, training, mentoring, team meetings, and organizational discussions • Record project time accurately each week

🎯 Requirements

• PhD in relevant scientific discipline, or master’s degree and at least three years of experience in a relevant field, or bachelor’s degree in a relevant scientific discipline and at least five years of experience in a relevant field • Outstanding analytical and problem-solving skills, including ability to assess quantitative data and draw appropriate conclusions • Excellent communication and scientific writing skills • Demonstrated ability to proactively and independently drive research projects • Ability and willingness to delegate and prioritize • Prior experience supporting patient-centered research studies (e.g., COA development and validation studies, ITR) • Proficient in MS Word, PowerPoint, and Excel • Experience in quantitative and/or qualitative data analysis desirable, with quantitative analysis particularly relevant to this role • Familiarity with statistical methods used in patient-centered research, clinical outcomes research, or COA evaluation • Experience with PubMed or similar literature databases advantageous • Ability to complete relevant training courses, follow SOPs and IRB requirements, and communicate effectively with clients

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