Clinical Data Standard Consultant

Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in statistics, computer science, mathematics, or related discipline
  • Experience in statistical programming within clinical research or pharmaceutical settings
  • Strong proficiency in SAS programming
  • Solid understanding of statistical concepts and methodologies
  • Excellent analytical and problem-solving skills with attention to detail
  • Strong communication skills for collaborative teamwork

Responsibilities

  • Develop and validate SAS programs for statistical analysis and reporting of clinical trial data
  • Collaborate with biostatisticians to define analysis plans and statistical methods
  • Perform quality control checks on statistical outputs
  • Assist in preparing statistical reports, presentations, and regulatory submissions
  • Identify efficiencies in programming processes for continuous improvement

Benefits

  • Various annual leave entitlements
  • A range of health insurance options for you and your family
  • Competitive retirement planning offerings
  • Access to a Global Employee Assistance Programme for well-being support
  • Life assurance
  • Flexible optional benefits including childcare vouchers and gym memberships
Full Job Description
Senior Statistical Programmer

A Principal Clinical Data Standards Consultant is responsible for supporting the operational staff in the use of ADaM and the define.xml capture for statistical analysis within the Medidata standard. They will develop tools to increase the efficiency, timeliness and quality of deliverables for data collection, tabulation, analysis and reporting. They will also define and collect metrics about the use of standards. They will participate in the development of training of the operational staff in the areas of their expertise.

What You Will Do:

Serve on Sponsor Standards and Technology Leadership teams.

Consult with clients on sponsor-specific CDISC centric implementation projects.

Participate in industry groups focused on the development of standards related initiatives (e.g. CDISC, PhUSE etc.).

Author, maintain, implement, and report status for Standards Related Project Plans.

Responsible for the implementation, strategy, and configuration of a metadata repository used to manage libraries of CDISC related metadata, terminology and related standards.

Mentor Clinical Data Standards Consultants. * Lead Subject Matter Expert teams on topics relevant to standards.

Identify areas for process improvement which may increase productivity, quality and / or compliance of deliverables in the areas from data collections through analysis and reporting.

Participate in the analysis of metrics and in creating recommendations to the management teams on process improvements together with the Director of Global Data Standards.

Your Profile:
• Minimum of 5 years of experience in industry in a role demonstrating knowledge of standards used by biometrics.
• An undergraduate degree or international equivalent from an accredited institution
• Demonstrated expertise in CDASH, SDTM standards and associated controlled terminology with a good understanding of CRF design concepts.
• Excellent communication skills with demonstrated leadership ability.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways


Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

About Pharmaceutical Research Associates, Inc

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