When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. 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 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 Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

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