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Principal Consultant, Real World Evidence (selected EU locations)

Employer
Parexel
Location
Hungary
Salary
Competitive
Start date
29 Mar 2021
Closing date
28 Apr 2021

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Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Job Description

The role can be office or home based in the selected EU locations.

The Principal Consultant, Real-world Evidence EU/UK is an experienced professional with proven study design, consulting, thought leadership and business development skills within the field of Real-world Evidence. This individual must have significant experience in the application of their expert knowledge to the design and successful delivery of real-world data studies which incorporate EMR, healthcare claims, patient registries, and other sources of secondary data for a variety of client-specific goals. The Principal Consultant, RWE EU/UK will support the overall growth of the team and business in the region, providing leadership and management in collaboration with the broader RWE and Access team.

Key Accountabilities:

Project Delivery
  • Ensure development of project plan detailing responsibilities, budgets, and timelines for any given RWE project
  • Guide clients on RWE data sets and how best to select the right data sources given the study question at hand
  • Lead analytical team including statistical programmers and epidemiologists to conduct variable creation, data manipulation and statistical analyses
  • As a project director, oversee the development of study protocol, analysis plans, and study reports as well as data analysis
  • Communicate with clients on a regular basis (project updates, results, discussion, present capabilities, discuss new potential projects)

  • Business Development and Thought Leadership
  • Active participation in the proposal development process through delivery of scientific data considerations (epi, stats, informatics, etc) for proposals and presentations at bid defenses
  • Development of industry network and identification of potential new business opportunities through networking and actively working with global sales team
  • Active participation in leading industry and academic forums and regular Thought Leadership contributions (e.g. presentations, articles, posters, etc.)
  • Provide analytical advice to peers and clients
  • Develop and manage client relationships
  • Develop and manage relationships with external data source organization as well as manage data access contracting and applications

  • Mentorship & Training
  • Provide guidance, training, and mentorship to all parts of the business involved in delivery of Real-world Evidence projects and services
  • Proactive mentoring of RWE team, including team supporting traditional site-based RWE studies
  • Qualifications

    Ideal candidate will possess:
  • Demonstrated expertise in RWE in the EU/UK, including support of proposal development and team building
  • Possess extensive knowledge of European secondary real-world data (RWD) sources such as claims, EMR, clinical databases, and other specialized data collection initiatives, ideally with existing relationships with these data holders.
  • Experience with end-to-end RWE project delivery focused on secondary data (RWD)
  • Recent Pharmaceutical / CRO/Consultancy experience
  • Master's degree or PhD in the area of outcomes research, epidemiology, biostatistics, statistics, health services research, or a related field, or equivalent professional experience
  • Highly effective communicator, both written and verbal, at all levels with customers, internally and with the industry at large
  • Comfortable operating in a demanding, fast-paced environment and capable of reacting swiftly to changing business demands
  • Driven to deliver quality results on time and in a highly ethical and professional manner
  • Consistent track record of successfully cultivating and managing client relationships
  • Strong client and project management skills on project director level
  • A high degree of written accuracy and attention to detail
  • Strong communication skills, especially in the relaying of technical information and project concepts
  • Fluent English, additional language would be an asset
  • Flexible, determined, and self-motivated
  • Why Work at Parexel

    There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?

    That's Parexel. We're a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.

    How can we help you on your journey? Find your path, and learn more on LinkedIn, YouTube, Facebook, Twitter, and Glassdoor.

    Company

    parexel

    When you join us, you’re joining a team that sees everything they do as an opportunity to transform the world for patients everywhere. When our employees bring their many perspectives together to tackle a new challenge, there’s no limit to what they can accomplish. Through it all, at the center of all we do, is a patient whose life could change – forever. And together, we’ll do it With Heart™.

    How to describe Parexel’s culture in one word: 

    Henry

     

     

    Working With Heart™ - Christina's perspective:

    Working With Heart™ - Christina's perspective:

     

    Careers Blog | Our Culture | Diversity, Equity & Inclusion | Benefits | Our Hiring Process

    Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory, and therapeutic expertise, our team of more than 21,000 global professionals works in partnership with biopharmaceutical leaders, emerging innovators, and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. 

    Company info
    Website
    Telephone
    +44 1895 238000
    Location
    The Quays
    101-105 Oxford Road
    Uxbridge
    Middx
    UB8 1LZ
    United Kingdom

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