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RWE Consultant - Sweden/Denmark

Employer
Parexel
Location
Sweden
Salary
Competitive
Start date
7 Dec 2022
Closing date
6 Jan 2023

View more

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

Job Details

We are recruiting for an RWE Consultant based in either Sweden or Denmark. who will provide a broad range of consulting services and works within projectguidelines to identify, refine, and address client issues and to achieve project objectives for our RWE portfolio. The Consultant providesoverall project leadership and provides guidance to project team members on technical and process issues

Key Accountabilities :
Accountability

Supporting Activities

Project Execution
  • Coordinate a project team of analysts to ensure timelydelivery 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.
  • 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 workprocess, specifically determining data structures andstatistical coding algorithms.
  • Follow comprehensive quality checking and validationprocesses.
  • Develop study protocols and define analytical variables collaboratively with external research scientists andbiostatisticians.


Business Development
  • Continuously develop existing processes to make more efficient and higher quality.
  • Lead development of data acquisition processes.
  • Control project out-of-scope activities with clients and manage contracting of change-in-scope.

Skills:
  • Strong project management skills.
  • Good presentation skills.
  • Process knowledge on primary data collection from sites.
  • 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, another European language will be a strong asset (preferably a Scandinavian language).

Knowledge and Experience :
  • A wealth of 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


Education:
  • Minimum Master’s degree (PhD preferred) in the area of outcomes research, epidemiology, biostatistics, statistics, health services research, or a related field

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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