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CDISC, a nonprofit organization dedicated to promoting clarity and impact in clinical research and global health, is looking for a Data Standards Lead to join their team. At CDISC, we value diversity and inclusion, creating an environment where all employees can learn from each other's unique strengths. By working together, we aim to drive more meaningful clinical research outcomes. If you are passionate about making a difference in the pharmaceutical industry and have expertise in CDISC standards, we invite you to apply for this exciting opportunity.

As the Data Standards Lead, you will be responsible for spearheading the strategic development of standards and initiatives that promote the adoption of CDISC standards across the industry. Working closely with internal data science, standards, and engineering teams, you will collaborate to enhance data interoperability and streamline processes. Additionally, you will engage with external stakeholders such as regulatory agencies, sponsors, and CROs to advance CDISC standards adoption. Your role will involve leading projects from initiation to completion while ensuring effective communication with development teams and stakeholders.

The ideal candidate for this position will hold a Bachelor's degree in computer science or a related field, along with a minimum of 3 years of professional experience in academic or pharmaceutical settings. You should possess a solid understanding of clinical data standards, end-to-end clinical development processes, and strong communication skills. Additionally, experience in cross-functional collaboration within matrixed organizations is preferred. If you have a Master's degree or 5 years of technical experience within relevant industries and proficiency with CDISC standards like Controlled Terminology, CDASH, SDTM, and ADaM - it would be considered an advantage.

Join us at CDISC as we continue to drive innovation in clinical research through the development of data standards that shape the future of healthcare worldwide. This position offers an excellent opportunity for individuals looking to make a significant impact on the pharmaceutical industry by leveraging their expertise in CDISC standards implementation. If you are ready to take on this challenge and contribute towards advancing transformation within the industry - apply now! This role is ideal for mid-career professionals seeking growth opportunities in data standardization leadership roles.

Key Job Requirements:
  • Minimum 3 years of professional experience in academic
  • CRO
  • regulatory settings
  • Bachelor's degree in computer science
  • informatics
  • public health or related field
  • Strong understanding of clinical data standards
  • Ability to work independently in a fast-moving environment
Key Job Responsibilities:
  • Lead the development, enhancement, and implementation of CDISC Standards
  • Collaborate cross-functionally with internal data science teams
  • Interact with external stakeholders to advance CDISC standards adoption
  • Assist with resource planning and coordination of project plans
Skills:
  • Clinical data standards knowledge
  • Communication skills
  • Strategic thinking
  • Problem-solving skills
  • Cross-functional collaboration

Seniority Level: Middle Management

  • Senior Level
  • Executive Level

Job Functions: Data Standards

  • Standards Development
  • Data Interoperability

Industries : Pharmaceutical

  • Healthcare
  • Clinical Research

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