Research Associate II, Patient Centered Research

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Execute fundamental project management responsibilities autonomously, encompassing financial oversight, scheduling, and client communication.

• Draft proposals, protocols, reports, and summaries.

• Synthesize results from both quantitative and qualitative analyses.

• Perform literature reviews and compile data from research articles.

• Gather qualitative data via cognitive interviews and by moderating or co-moderating focus groups.

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

• Conduct qualitative and quantitative data analyses, including the preparation of codebooks, coding, and reviewing data tables.

• Stay updated with current scientific literature.

• Collaborate as a co-author on scientific presentations and journal articles.

• Manage and oversee site recruitment, site administration, site training, and data management processes.

• Delegate tasks and facilitate communication within and beyond project teams.

• Supervise project budgets, PDR and achievement reports, invoices, and financial records.

• Monitor project timelines and ensure project teams are kept informed.

• Oversee and manage IRB submissions, documentation, SOP requirements, and business office procedures.

• Liaise with clients and senior project team members regarding project responsibilities, budgets, and timelines.

• Conduct and present internal scientific training and participate in training led by colleagues.

• Adhere to SOPs and Evidera training protocols.

⛳️ Requirements

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

• Proficiency in Microsoft Word, PowerPoint, and Excel.

• Familiarity with EndNote, PubMed/Embase, ATLAS.ti, and Access with provided interfaces.

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

• Practical experience in implementing research projects.

• Knowledge of IRB processes, data collection and management, as well as qualitative and quantitative analysis.

• Strong communication and scientific writing abilities.

• Excellent problem-solving, analytical, and attention-to-detail skills.

• Capable of working efficiently within diverse project teams and managing multiple tasks.

• Evidence of scholarly work through peer-reviewed publications, technical reports, or similar scholarly contributions.

• Competence in performing standard and routine office tasks.

• Willingness and ability to travel domestically and internationally 10–30% of the time.

🏝️ Benefits

• Competitive salary.

• Annual incentive bonus plan.

• Comprehensive healthcare coverage.

• A wide array of employee benefits.

• Opportunities for career advancement and development.

• Professional development and training through participation in scientific conferences.

• A culture that is innovative and forward-thinking.