Senior Associate, Clinical Outcomes Assessment
United States of America, Remote Job ID R0000029675 Category Regulatory / Consulting Date Posted 11/22/2024Overview
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
We are currently seeking a Senior Associate, Clinical Outcomes Assessment to join Parexel's growing team. This role offers a unique opportunity to support our team of clinical outcome assessment (COA) scientists in the evaluation of discrete event modelling made with patient input. The existing team includes psychologists with a broad range of experience in industry, academia and clinical practice.
As a Senior Associate, Clinical Outcomes Assessment, you will be responsible for COA projects on Instrument validation, Implementation and COA Analyses, Qualitative Interview Studies as well as, potentially, Preference designs including Discrete Choice Experiment survey design and providing strategic input and advice to our clients.
Key responsibilities:
Support Qualitative interviews with Patients, Clinicians and Caregivers, ePRO vendor oversight, Psychometric Validation analyses, Patient Preference and DCE projects.
Design, conduct, and analyze psychometric as well as health-related user preferences studies.
Advocate behavioral science methods more broadly across the Parexel and clients and generalize learnings into a framework that can help bring behavioral science to scale.
Develop proposals and study protocols that include elements of experimental design.
Qualifications:
Ideally a recognized or up and coming expert in the field of COA implementation or validation, demonstrated through publication records, involvement in relevant special interest groups (e.g. ISPOR, ISOQOL).
Minimum of 3-4 years’ experience in COA Validation and Psychometrics, as established by publication records.
Strong scientific and regulatory knowledge of relevant guidelines.
Minimum MSc, PhD preferred in a relevant discipline (e.g. Psychology, Statistics, Outcomes Research).
Fluent in vocal and written English.
Additional languages – highly desirable i.e. Spanish
East Coast Candidates Highly Preferred
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EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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