Senior Health Economics Associate
- Location India-Hyderabad-Remote
- Experience 3+ yrs
- Job type Full-time
- Posted 8 Oct 2026
You will be taken to the employer’s own careers page to apply.
Job details
- Qualification
- Master's
- Job ID
- R0000044811
Job description
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.