Biomarker Operations Specialist — Clinical Trials

Crispr Therapeutics AG

Boston (MA)

Hybrid

USD 85.000 - 100.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Remote work flexibility
On-site collaboration

Zusammenfassung

CRISPR Therapeutics is seeking a Specialist in Biomarker Operations based in South Boston, MA. The role supports PK/PD and translational biomarker workflows, coordinating with vendors, central labs, and CROs to ensure timely sample processing and data transfer.

The ideal candidate has a BS in a related field with 3–5+ years in clinical trial operations or biospecimen management, with strong organization, attention to detail, and knowledge of GCP.

Qualifikationen

  • BS in related field with 3–5+ years of experience in clinical trial operations, biospecimen management, or lab operations.
  • Strong organizational skills with high attention to detail and accuracy.
  • Familiarity with GCP and biospecimen handling regulations.

Aufgaben

  • Identify vendors to support program-specific biomarker needs.
  • Collaborate with Clinical Pharmacology leads on vendor selection, scope-of-work, and budget review.
  • Coordinate data transfer agreements and track data transfers against study timelines.
  • Ensure sample handling adheres to GCP and regulatory requirements.
  • Serve as a key liaison between Clinical Pharmacology, Clinical Operations, Data Management, and external labs.

Kenntnisse

Organizational skills
Attention to detail
Project coordination

Ausbildung

Bachelor's degree
Advanced degree

Tools

Oracle
Conga

Jobbeschreibung

CRISPR Therapeutics is seeking a Specialist in Biomarker Operations based in South Boston, MA. The role supports PK/PD and translational biomarker workflows, coordinating with vendors, central labs, and CROs to ensure timely sample processing and data transfer.

The ideal candidate has a BS in a related field with 3–5+ years in clinical trial operations or biospecimen management, with strong organization, attention to detail, and knowledge of GCP.

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