Research Associate II, Patient Centered Research

This is a fully remote position, open to applicants in United Kingdom, +4 more countries.

📋 Description

• Prepare proposal drafts, protocol drafts, and reports/summaries independently.

• Summarize results of quantitative and qualitative analyses.

• Conduct literature reviews and organize data from articles.

• Collect qualitative data, including conducting cognitive interviews and moderating or co-moderating focus groups.

• Handle data management, data entry, and data review tasks.

• Perform qualitative coding and review tables of quantitative data.

• Stay updated with current scientific literature.

• Co-author scientific presentations for conferences and journal manuscripts when applicable.

• Manage site recruitment, site management, site training, and data management.

• Delegate tasks and communicate effectively within and outside the project team.

• Supervise project budgets, review reports, approve and track invoices from subcontractors and clients, and maintain the project checkbook.

• Monitor timelines and keep the project team informed of progress.

• Oversee and manage IRB submissions, filing, SOP requirements, and business office practices.

• Engage with clients and senior project team members regarding project tasks, budgets, and timelines.

• Manage and deliver internal scientific training sessions.

• Participate in colleague-led training and adhere to SOPs and Evidera training requirements.

• Travel 10–30% of the time.

⛳️ Requirements

• MA/MS with over two years of experience, or BA/BS with more than three years of experience, or an equivalent background in outcomes research, clinical trial execution, or human subjects research.

• Proficient in MS Word, PowerPoint, and Excel.

• Experience with EndNote, PubMed/Embase, ATLAS.ti, and capable of using Access with provided interface.

• Understanding of health outcomes/human subjects research principles and good clinical practices.

• Practical knowledge of implementing research projects.

• Familiarity with IRB processes, data collection and management, and both qualitative and quantitative analysis.

• Strong communication, problem-solving, attention to detail, teamwork, multitasking, analytical, and scientific writing skills.

• Proven scientific writing experience through peer-reviewed publications, technical reports, or other scholarly work.

• May require domestic and international travel.

🏝️ Benefits

• Competitive remuneration.

• Annual incentive plan bonus.

• Healthcare coverage.

• A variety of employee benefits.

• Career advancement and development opportunities.

• Professional development/training through potential attendance at scientific conferences.