Evidence Evaluation Analyst (Health Economics and Outcomes Research Specialist, Systematic Review Coordinator)

Parexel

As part of Parexel Consulting, you will play a vital role in helping biopharmaceutical and medical device companies navigate the complex and ever-changing regulatory landscape. Drawing on your scientific, technical, and regulatory expertise, you will work closely with clients to develop and implement regulatory strategies that bring their products to market faster and keep them there.

We value collaboration, innovation, and continuous learning. As a member of our team, you will partner with a diverse group of clients, and be exposed to various product types and therapeutic areas. You will also develop your skills through challenging assignments and mentorship from experienced regulatory professionals. Plus, you will enjoy the flexibility of working remotely while still being part of a supportive and dynamic team.

Success Profile

Do you have these soft skills and interpersonal traits to succeed at Parexel?

• Communicator
• Detail-oriented
• Problem-solver
• Relationship-builder
• Results-driven
• Strategic

About This Role

About Parexel

Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose – moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart®.

About the Role

We are seeking an Evidence Evaluation Analyst (Health Economics and Outcomes Research Specialist, Systematic Review Coordinator) to join our Evidence Evaluation team in a remote capacity. As an Evidence Evaluation Analyst, you will execute end-to-end Systematic Literature Reviews (SLRs) and produce high-quality evidence deliverables that advance clinical knowledge and support informed decision-making in healthcare. This position plays a key role in generating rigorous evidence synthesis, supporting regulatory submissions, and contributing to clinical research that improves patient outcomes.

You'll collaborate with Project Leads, Technical Subject Matter Experts, and cross-functional teams to deliver client-ready outputs including systematic review reports, manuscripts, abstracts, posters, and presentations. Following industry-standard methodologies and evidence evaluation best practices, you'll contribute to project execution from protocol design through final deliverable production.

You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through rigorous evidence synthesis, high-quality deliverable development, and strategic client engagement. With diverse teams and continuous learning opportunities, the Evidence Evaluation Analyst can explore career paths and expand skills across health economics, outcomes research, and clinical evidence generation.

Key Responsibilities

• Execute systematic literature review steps including protocol design, literature screening, data extraction, and quantitative feasibility assessments
• Develop high-quality SLR deliverables such as systematic review reports, slide decks, manuscripts, abstracts, and posters tailored to client specifications
• Conduct comprehensive literature searches, study selection, and data synthesis to support evidence generation
• Work effectively both independently and within team structures under guidance from Project Leads and Technical SMEs to deliver client-ready outputs
• Prioritize tasks, align with project managers, and maintain quality standards while meeting project timelines
• Interact professionally with clients at all organizational levels and support presentations with senior guidance
• Support Project Leads with project management tasks, customize deliverables as required, and identify process improvements
• Support the development of health economics and outcomes research proposals and identify potential new business opportunities
• Meet organizational scorecard metrics, complete core responsibilities including timesheets and documentation, and pursue self-development activities to stay current in the evidence evaluation field

You'll thrive in this role if you bring:

• Strengths in systematic literature review methodology, evidence synthesis, and data analysis

• Experience executing SLR steps including screening, data extraction, and report development

• The ability to collaborate across teams, manage stakeholder relationships, and communicate clearly with diverse audiences

• A patient-focused mindset, commitment to research quality, and strong attention to detail

• Comfort working with literature review tools, data management systems, and Microsoft Office Suite

• Self-motivation, enthusiasm, and flexibility to adapt to evolving project needs

• Required Qualifications

• Bachelor's degree in a Scientific or Technical discipline

• Strong communication, organization, and problem-solving skills

• Experience working in clinical research, healthcare, outcomes research, or a regulated environment

• Knowledge of evidence synthesis methodologies and clinical trial processes

• Ability to manage multiple tasks, prioritize effectively, and deliver high-quality work independently

• Preferred Qualifications

• Master's degree in Life Sciences, Public Health, Health Economics, or related field

• More than 3 years of relevant experience in health economics and outcomes research (HEOR) or systematic literature reviews

• Postgraduate degree in COA-related fields such as Psychology, Social Science, or Anthropology

• Experience with literature review software, data management platforms, or statistical analysis tools

• Familiarity with regulatory guidelines and health technology assessment (HTA) methodologies

• Project management experience or business development support

• Employee Insights

• How to describe Parexel culture in one word

• Insights from Parexel employees

• Watch Video

• Jo on diverse project work and team culture

• Jo Wang | Vice President, Technical

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• Kurt on colleagues and growth opportunities

• Kurt Brorson | Vice President, Technical

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• Why Consultants work at Parexel

• Patient-led in everything we do

• We are inspired by the patients behind the data and therefore deliver first-time quality and on-time projects.

• Supportive and inclusive environment

• We thrive on collaboration, caring, and inclusivity - enabling our people to work together to solve complex problems and share knowledge.

• Opportunities for career growth

• We provide a wide range of challenging assignments, product types, geographic regions, and therapeutic areas, providing ample opportunities for learning and growth.

• Flexible work arrangements

• We offer the flexibility of remote work, allowing you to balance your personal and professional responsibilities while still contributing to our “We Care” team environment.

• Diverse and global client exposure

• We continuously learn by working with a global network of colleagues and clients to develop regulatory strategies to support their product development and approval.

• Learn from experts

• You will work with a team of highly experienced regulatory professionals who can serve as mentors, providing guidance and support as you develop your skills and advance in your career.

• Learn About Our Culture

• Cell and Gene

• Our Cell and Gene Therapy Center of Excellence (COE) integrates regulatory expertise with a cross-functional team to get treatments to market faster.

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• General Medicine

• Our general medicine thought leaders provide innovative development strategies and principled trial design and conduct across the following indications: Cardiovascular, Endocrinology and metabolism, Nephrology and genito-urinary, Respiratory, and Women’s health.

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• Hematology

• Our specialists in hematology have long been at the cutting edge of innovations, treating patients participating in clinical trials from first-in-human to post-market studies across the indications of Lymphoma, Acute myeloid leukemia (AML), Myelodysplastic syndrome (MDS), Multiple myeloma, Benign and malignant disorders.

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• Infectious Disease and Vaccines

• Our infectious disease team is built upon the global experience and public health knowledge that drives research within these indications: Hepatitis B, Bacterial indications, Vaccines, preventative, and treatment, Critical care, Long COVID syndrome.

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• Inflammation and Immunology

• Our broad knowledge of the underlying mechanisms of diseases, paired with m