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Senior Statistical Programmer
drjobs Senior Statistical Programmer العربية

Senior Statistical Programmer

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1 Vacancy
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Jobs by Experience

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1 - 0 years

Job Location

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Manama - Bahrain

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Nationality

Any Nationality

Gender

N/A

Vacancy

1 Vacancy

Job Description

Req ID : 2609202

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

What you will be doing:

  • Extract clinical data from the clinical data management system and produce standard and custom reports, primarily in
  • Program reports and listings as requested by project team members for ongoing studies.
  • Develop transfer specifications with vendors for external data sources.
  • Perform consistency checks on data transferred between internal and external parties to ensure completeness and accuracy of data contained
  • Perform programming to convert raw, clinical trial data to Study Data Tabulation Model (SDTM) format .
  • Perform Quality Control (QC) on programming work performed by fellow Database
  • Create and validate global macros or systems that streamline repetit ive operations to increase programming efficiency.

You possess:

  • Bachelor's degree in Healthcare field, Biology, Statistics or
  • Minimum of 5 years of clinical SAS programming experience in the pharmaceutical industry.
  • Working knowledge of CDISC SDTM mapping/specs/conversion/domains/datasets/eCRF/eCRT Package/define.xml development and SDTM data transfer operations on clinical studies.
  • Understanding of regulatory requirements relevant to submissions .
  • Knowledge of clinical trial study design and electronic data submission
  • Communication and interpersonal skills and the ability to work effectively as part of a team.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON:

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Employment Type

Full Time

Department / Functional Area

Administration

Key Skills

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