As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small.
In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of Parexel Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.
- Full Time
- Level: Mid
- Travel: Yes
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Success Profile
Check out the top traits we're looking for and see if you have the right mix.
- Detail-Oriented
- Proactive
- Problem-Solver
- Results-Driven
- Organized
- Multi-Tasker
Rewards
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Global Impact
We are one truly global team working together to propel each client´s journey ahead faster.
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Balance
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
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Collaboration
Work with industry leaders and subject matter experts.
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Freedom
The ability to innovate, ask “what if” and try new solutions without fear of failure.
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Variety
Opportunities to work on multiple accounts – never boring!
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Management
Strong management with depth of experience working for global health authorities.
Responsibilities
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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