Senior Statistical Programmer

Moscow, Russia
26 Feb 2021
12 Mar 2021
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Job Description

Essential Function
The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Programmer can fill the Statistical Programming Coordinator role on projects, and liaise with sponsors, Data Operations Leads, and other functional areas as required. General areas of responsibility also include: import/export programming specification development, test data creation and test data entry, import/export programming functional testing, as well as mapping specifications to support relevant data standards.Qualifications

* Proficiency in SAS.
* Knowledge of the programming and reporting process.
* Knowledge of WSOP's/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.
* Demonstrate ability to learn new systems and function in an evolving technical environment.
* Strong leadership ability.
* Attention to detail.
* 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.
* 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.
* Shows commitment to and performs consistently high quality work.

* Educated to degree level in a relevant discipline and/or equivalent work experience.

Language Skills
* Competent in written and oral English.
* Excellent communication skills.

Minimum Work Experience
* Relevant Clinical Trial industry 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.

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