Sr. Associate, Clinical Data Operations

Scorpion Therapeutics

United States

Remote

USD 70,000 - 90,000

Full time

14 days+
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Job summary

Scorpion Therapeutics is seeking a Senior Clinical Data Operations Associate to support bio/pharma and academic clinical trials. You will manage study documentation, monitor sample processing, and help ensure data quality.

Remote-first role based in the Boston area, with travel not specified; you will collaborate across teams to resolve queries, maintain compliance with GxP, HIPAA, and GCP, and contribute to process improvements and training.

Qualifications

  • Bachelor's degree in a scientific field or equivalent; 1+ years experience, 4+ preferred, knowledge of oncology, molecular biology, genetics or bioinformatics.

Responsibilities

  • Manage study documentation.
  • Monitor sample processing and reporting.
  • Oversee query resolution.
  • Ensure data quality and compliance with GxP, HIPAA and GCP standards.
  • Coordinate sample return/destruction.
  • Contribute to process improvement and training.

Skills

Advanced data QC
Programming basics
Process implementation
Strong communication
GCP experience
Study documentation
Cross-team collaboration

Education

Bachelor's in a scientific field

Job description

Role: Senior Clinical Data Operations Associate supporting bio/pharma and academic clinical trials; focuses on sample tracking, data management, and operational support.

Responsibilities
  • manage study documentation
  • monitor sample processing and reporting
  • oversee query resolution
  • ensure data quality and compliance with GxP, HIPAA, and GCP standards
  • coordinate sample return/destruction
  • and contribute to process improvement and training.
Qualifications
  • Bachelor's in a scientific field or equivalent, with 1+ years of experience; preferred 4+ years, with knowledge of oncology, molecular biology, genetics, or bioinformatics.
Skills
  • advanced data QC, programming basics, process implementation, and strong communication
  • experience in GCP, study documentation, and cross-team collaboration is valued

Work setup primarily remote in Boston; other details on travel are not specified.

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