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Research Associate II, Patient Centered Research

🔥 13 hours ago

🌐 United Kingdom, France, +3 more countries – Remote

infoinfo

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

Where this job comes from

Posted on Thermo Fisher Scientific's careers page, not through a job board

First seen by Remote Rocketship 13 hours ago

Still open on Thermo Fisher Scientific's site. Checked 0 minutes ago.

Logo of Thermo Fisher Scientific

Thermo Fisher Scientific

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

• Independently prepare proposal drafts, protocol drafts, and reports/summaries • Summarize quantitative and qualitative analysis results • Conduct literature reviews and tabulate data from articles • Collect qualitative data, including conducting cognitive interviews and moderating or co-moderating focus groups • Perform data management, data entry, and data review • Conduct qualitative coding and review quantitative data tables • Maintain familiarity with current scientific literature • Co-author scientific conference presentations and journal manuscripts when applicable • Oversee and conduct site recruitment, site management, site training, and data management • Delegate and communicate within and outside the project team • Oversee project budgets, review reports, approve and track subcontractor and client invoices, and maintain the project checkbook • Track timelines and keep the project team informed • Oversee and manage IRB submissions, filing, SOP requirements, and business office practices • Communicate with clients and senior project team members about project tasks, budgets, and timelines • Manage and present internal scientific trainings • Attend colleague-led trainings and comply with SOPs and Evidera training requirements • Travel 10–30% of the time

🎯 Requirements

• MA/MS with more than two years of experience, or BA/BS with more than three years of experience, or equivalent thereof in outcomes research, clinical trial execution, or human subjects research • Proficiency with MS Word, PowerPoint, and Excel • Experience with EndNote, PubMed/Embase, ATLAS.ti, and ability to use Access with interface provided • Knowledge of health outcomes/human subjects research principles and good clinical practices • Practical knowledge of research project implementation • Knowledge of IRB processes, data collection and management, and qualitative and quantitative analysis • Good communication, problem-solving, attention to detail, teamwork, multitasking, analytical, and scientific writing skills • Scientific writing demonstrated by peer-reviewed publications, technical reports, or other scholarly work • May require domestic and international travel

🏖️ Benefits

• Competitive remuneration • Annual incentive plan bonus • Healthcare • Range of employee benefits • Career and development prospects • Professional development/training through possible scientific conference attendance

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