Health Economics Jobs » United Kingdom » Senior Consultant, RWE

Senior Consultant, RWE

Home-based, UK.

A Senior Consultant:

* provides a broad range of consulting services and works within project guidelines to identify, refine, and address client issues and to achieve project objectives.
* serves either as an individual contributor, a workstream lead or provides overall project leadership.
* provides guidance to project team members on technical/process issues.

Key Duties:

• Coordinate a project team of analysts to ensure timely delivery of projects to a high standard, managing client communications, and ensuring projects are delivered on budget. Including project planning and execution.
• Coordinate real-world data collection processes from sites and data register.
• Lead client engagements activities. To advise clients on their needs as well act as the main Parexel client contact during the project. Contributes idea for approaches to new clients or new service offerings.
• Provide technical leadership and training to more junior staff within the team, and ensure own skills are up to date; contribute to thought leadership initiatives.
• Apply data analytics to support research projects and collaborations within the team. This will include supervising the conduct of statistical analyses, analytic datasets creation, and performing quality control.
• Leading development study protocols, statistical analysis plans and coaching the team through the analytical work process, specifically determining data structures and statistical coding algorithms.
• Follow comprehensive quality checking and validation processes.
• Develop study protocols and define analytical variables collaboratively with external research scientists and biostatisticians.


• A minimum of 8 years’ experience working with in real-world evidence, with particular emphasis on large relational databases, processing large administrative healthcare datasets (medical and pharmacy claims), and or clinical databases (Electronic Health Records), creating final analytical databases, conducting secondary data analyses, and developing research study designs.
• Recent Pharmaceutical/CRO experience preferred.
• Experience in Real World Evidence, epidemiology, or register studies.
• Past experience in the development of real world evidence proposals is an advantage.
• Demonstrated evidence of publications will be viewed favorably.
• Minimum Master’s degree (PhD preferred) in the area of outcomes research, epidemiology, biostatistics, statistics, health services research, or a related field.

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.

This job is posted by Parexel.


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