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Senior Statistical Programmer (Data Visualization/RWE) UK/EU

Employer
Parexel
Location
Czech Republic
Salary
Competitive
Start date
2 Jun 2021
Closing date
2 Jul 2021

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

Job Details

Job Description

.*We are currently seeking an experienced Senior Statistical Programmer (Real World Evidence / Data Visualization) to work Home-Based in either the UK or other selected EU locations (Eastern Europe countries). We are looking for an epidemiological/statistical programmer to work in a Functional Programming group. The role involves producing analysis datasets using SAS and creating visualizations from these datasets using Spotfire as well as ad-hoc analysis work. Candidates must be comfortable with creating complex analysis datasets derived from large databases and have a careful eye for outliers and errors. This will include checking the accuracy of programs written by colleagues. The role will involve interpreting plans of analysis developed by epidemiologists. At times the successful candidate will need to deliver results within short timelines and on occasion will need to balance more than one study at a time. The ability to work effectively and successfully in a team environment, strong documentation, communication and time management skills are essential. The team works using Agile methodology. The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Programmer can fill the Statistical Programming Lead role on projects, and liaise with sponsors, Biostatistics Leads, Data Management Leads, and other functional areas as required. Further, the Senior Statistical Programmer will monitor quality, timelines, resource allocation, and productivity in relation to budgets.Qualifications

.The preferred candidate will have knowledge of SAS programming skills, however candidates without SAS knowledge but with knowledge of R or Python will also be considered. Candidates will need to have a programming background. Knowledge of SQL is needed. Applications from candidates with experience of working with Spotfire are encouraged. Candidates with experience of working with observational data and with epidemiological knowledge will be favoured. The main skills we are looking for however are the ability to interpret and clarify the details of a plan of analysis and to implement the programming necessary to deliver the results requested. Communication is key in this role.
Additional skills for a Senior Programmer
• 6 or more years programming at a Pharma company
• MSc required
• Working with large databases is essential
• Candidates would be expected to lead projects soon after starting

Other:-
• Excellent analytical skills with sound Lead experience as a Statistical Programmer within the Clinical Research (CRO) environment is essential.
• Excellent analytical skills.
• Proficiency in SAS.
• Extensive knowledge and understanding of the programming and reporting process.
• Knowledge of SOP's/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11.
• Ability to learn new systems and function in an evolving technical environment.
• Strong project management skills.
• Strong organizational skills, ability to manage competing priorities, and flexibility to change.
• Attention to detail.
• Ability to successfully lead a global team.
• Work effectively in a quality-focused environment.
• Effective time management in order to meet daily metrics or team objectives.
• Show commitment to and perform consistently high quality work.
• Business/operational skills that include customer focus, commitment to quality management, and problem solving.
• Demonstrate commitment to refine quality processes.
• Good presentation skills.
• Good business awareness/business development skills (including financial awareness).

Knowledge and Experience:
• Competent in written and oral English.
• Excellent communication skills.

Experience with real world healthcare data such as DRG, MarketScan, Optum, PharMetrics, Medicare and EMR databases.

Education:
• Educated to degree level in a relevant discipline and/or equivalent work experience.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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