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Principal Statistical Programmer - FSP

Not Specified, United Kingdom, £ £ - Annual Annual, Permanent

Description:

*Job Description*

The Principal Statistical Programmer (FSP) will be recognized as a subject matter expert, providing technical support and expert advice to internal and external sponsors, and works independently to support various programing activities related to the analysis and reporting of clinical study data. In addition, the Principal Statistical Programmer can fill the Primary Statistical Programmer role on projects and liaise with sponsors, Data Operations Leads, and other functional areas as required. Furthermore, the Principal Statistical Programmer will monitor quality, timelines, resource allocation, and productivity in relation to budgets.
*Qualifications*

* Proficiency in SAS
* Proven Lead Statistical Programming experience within related environment (minimum 6 years experience)
* Knowledge of the programming and reporting process
* Knowledge of WSOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application
* Demonstrated application of CRS concepts to achieve best practice and promote continuous improvement
* Demonstrate ability to learn new systems and function in an evolving technical environment
* Strong leadership ability.
* Ability to successfully work together with a ("virtual") team (including international teams as required) as well as independently
* Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to change
* Attention to detail.
* Excellent analytical skills.
* Good presentation skills.
* Tenacity to work in an innovative environment.
* Ability to negotiate and influence in order to achieve results.
* Business/Operational skills that include customer focus, commitment to quality management and problem solving.
* Good business awareness/business development skills (including financial awareness).
* Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
* Work effectively in a quality-focused environment.
* Demonstrate commitment to refine quality processes.
* Effective time management in order to meet daily metrics or team objectives
* Show commitment to and perform consistently high quality work
Education* Educated to degree level in a relevant discipline and/or equivalent work experience
Language Skills* Competent in written and oral English.
* Excellent communication skills.
*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.

Job Details

1342300749
Sat, 18 Sep 2021 19:00:00 EST
Not Specified
Not Specified, United Kingdom
Permanent
£ £ - Annual Annual