R

Rho

Comprehensive CRO for regulatory drug approvals

Clinical Data Associate

Clinical Research OperationsPosted on Nov 10
Full-timeRemote in PolandNo salary listed

About the Job

Requirements

  • A Bachelor's degree, preferably in Engineering, Mathematics, Computer Science, or Statistics.
  • Strong computer skills and working knowledge of Microsoft Word, Excel, PowerPoint, and Adobe Acrobat.
  • Strong interest in data and statistical analysis.
  • Demonstrated written, verbal, and presentation skills.
  • Attention to detail and ability to uphold high-quality scientific standards.
  • Honesty and integrity, with accountability and respect for colleagues.
  • Ability to evaluate situations objectively and develop practical solutions.
  • Ability to adapt quickly to changes.

Responsibilities

  • Review protocols and apply protocol-specified guidelines to the structure, review, and cleaning of clinical data.
  • Support study setup, including EDC build (forms, edit checks, and study structure) and validation user acceptance testing.
  • Contribute to EDC validation user acceptance testing, including forms, edit checks, study structure, custom functions, and integrations.
  • Program basic SAS manual data review and data reconciliation listings.
  • Review data reconciliation listings to identify data discrepancies and necessary queries or follow-up.
  • Issue and manage queries in the EDC database under the oversight of the Lead Data Manager.
  • Review data visualizations and listings to identify discrepancies, track trends, and identify areas of concern or risk; bring identified issues or risks to the cross-functional study team with oversight support from the Lead Data Manager.
  • Work closely with Lead Data Managers and other lead project team members to support project execution and sponsor satisfaction.

About the Company

Rho

Comprehensive CRO for regulatory drug approvals

Rho is a contract research organization that provides end-to-end services for developing and gaining regulatory approval for drugs, biologics, and medical devices. It supports planning and executing clinical development, regulatory strategy, and marketing submissions, guiding projects from program strategy through NDAs, BLAs, and MAAs. An integrated team handles decentralized clinical trials and has infectious-disease programs, combining trial design, data management, and regulatory insight to move products toward approval. Its goal is to help clients bring products to market efficiently by navigating regulatory requirements and streamlining development and submission processes.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Durham, NC
Founded
1984

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