Research Associate III – Clinical Outcomes Assessment

🔥 12 hours ago

🇲🇽 Mexico – 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 • 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 • Conduct qualitative interview studies and/or surveys with patients, caregivers, and investigators • Contribute to quantitative survey design, 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 data quality control • Conduct descriptive and inferential analyses, review analysis outputs, and interpret findings • Contribute to scientific dissemination through manuscripts, posters, and conference presentations • Contribute to broader Patient-Centered Research team projects • Track project timelines and budget use with the Project Management Office • Communicate effectively with clients and project teams • Stay current with relevant research and contribute to PCR initiatives, training, mentoring, and organizational discussions • Record project time accurately each week

🎯 Requirements

• PhD in a 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 the 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, such as COA development and validation studies or ITR • Proficiency in MS Word, PowerPoint, and Excel • Experience in quantitative and/or qualitative data analysis desirable, with quantitative analysis particularly relevant • 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, including adverse event training, SOPs, and ethics • Familiarity with electronic filing requirements, relevant SOPs, and IRB needs

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule • Opportunities to grow scientific knowledge and consulting skills • Opportunity to collaborate with a wide range of study sponsors • On-the-job learning opportunities • Mentorship and participation in training initiatives

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