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Job Details

Statistical Programmer II (Germany, Berlin)

Company: PAREXEL
Location: Berlin, Land Berlin,Germany
Reference: 41996BR
Closing Date: 26 May 18
Type: Not Specified
Salary (£): Competitive
Benefits:

Job Summary:

At PAREXEL, we believe that the power to work independently and intelligently should be yours every day.Your ability to understand our clients’ needs and achieve quality results is critical to our reputation as one of the best clinical research organizations (CROs) in the world. ...

Requirements:

At PAREXEL, we believe that the power to work independently and intelligently should be yours every day.
Your ability to understand our clients’ needs and achieve quality results is critical to our reputation as one of the best clinical research organizations (CROs) in the world. PAREXEL Statistics teams have an excellent reputation in the industry for their standards of work and quality of results
As a Statistical Programmer dedicated to one of our clients, you will be involved in 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. You will have the opportunity to become a subject matter expert for specific tasks within a key client partnership and to become involved in business development activities.

An exciting and rewarding opportunity has arisen to join our international team as

Statistical Programmer II


The Statistical Programmer II provides technical expertise for the conduct of clinical trials, and works with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data. 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.

You’ll be able to develop your statistical skills, developing yourself towards a functional lead role in our dynamic teams. You’ll gain exposure to multiple therapeutic areas, have the opportunity to grow and develop your career and be part of a pleasant and flexible working environment.

Key Accountabilities

  • Ensure quality control (QC) on all process and technical activities related to derived dataset, table, listing, and figure programming in accordance with corporate quality standards, WSOPs/Guidelines, ICH-GCP and/or other international regulatory requirements are performed.
  • Assist in the coordination of project start-up activities, including Unix/PMED project area set-up, creation of global programs (e.g. setup.sas, formats.sas, etc.), tracking spreadsheets, and required documentation.
  • Assist in the production and QC of derived dataset specifications, programming specifications, and other process supporting documents.
  • Use efficient programming techniques to produce derived datasets, tables, figures and data listings of any complexity and QC low-medium complexity derived datasets, tables, figures and data listings.
  • Develop wider knowledge of SAS and other relevant programming languages and processes within the GRO, Biostatistics, and Medical arenas.
  • Assist project teams in the resolution of problems encountered in the conduct of their daily work.
QualificationsSkills
  • Proficiency in SAS.
  • 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.
  • Demonstrate ability to learn new systems and function in an evolving technical environment
  • 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.
  • 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.
Education
  • First degree (undergraduate or equivalent) in a relevant discipline is preferred or equivalent work experience.
Language Skills
  • Competent in written English.
  • Good communication skills.
Minimum Work Experience
  • Relevant Clinical Trial industry experience.
Starting your journey with PAREXEL comes along with an extensive induction program and ongoing training while following your individual career path. On your PAREXEL journey, you will be involved in all statistical aspects of clinical trials, you will work in cross-functional teams, and with managers who know your strengths. If you’re looking for flexibility and work-life balance, we’re here to listen and help you move forward with your individual career path.
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. If you’re looking to collaborate with life science industry leaders, gain exposure to industry changing technology, and find the security of a role within a global CRO join a team that will help you move forward with your individual career path.

Apply for this job: Statistical Programmer II (Germany, Berlin)

Contact Information:

Address:  PAREXEL International
The Quays
101-105 Oxford Road
Uxbridge
Middlesex
UB8 1LZ
England
Tel:  +44 1895 238000
Fax:  +44 1895 238494
Website:  Visit Our Web Site
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