Biomarker Operations Specialist – Clinical Trials

CRISPR Therapeutics, Inc.; Boston (MA); Hybrid; USD 85.000 - 100.000; Vollzeit

Benefits dieser Stelle

On-site 3 days/week

Bonus program

Equity

Benefits

Zusammenfassung

CRISPR Therapeutics, Inc. in Boston, MA seeks an experienced Specialist to support the Clinical Pharmacology department.

You will manage lifecycle data flows for biospecimens in clinical trials, coordinating with vendors, labs, and data management to ensure timely sample processing and data transfer. The ideal candidate has 3–5+ years in clinical trial operations or biospecimen management, strong organizational skills, and working knowledge of PK/PD and biomarker assays.

Qualifikationen

• BS in related field with 3-5+ years in clinical trial operations, biospecimen or lab operations; advanced degree can substitute years of experience.
• Strong organizational skills with attention to detail and accuracy.
• Familiarity with PK/PD, immunogenicity, biomarker assay types.
• Experience coordinating budgets, vendors, and cross-functional teams.

Aufgaben

• Provide operational support for PK, PD, and translational biomarkers.
• Identify and vet vendors for program biomarker needs.
• Collaborate with Clinical Pharmacology Leads on vendor scope, SOA, and budgets.
• Coordinate contracting with Finance and Legal; manage timelines for data transfers with labs/CROs.
• Liaise with central labs, biorepositories, and CROs to ensure timely sample processing and data transfer.

Kenntnisse

Clinical trial operations

Biospecimen management

Documentation & regulatory

Vendor management

Cross-functional collaboration

Ausbildung

BS in related field

Advanced degree

Tools

Oracle

Conga

Jobbeschreibung

CRISPR Therapeutics, Inc. in Boston, MA seeks an experienced Specialist to support the Clinical Pharmacology department.

You will manage lifecycle data flows for biospecimens in clinical trials, coordinating with vendors, labs, and data management to ensure timely sample processing and data transfer. The ideal candidate has 3–5+ years in clinical trial operations or biospecimen management, strong organizational skills, and working knowledge of PK/PD and biomarker assays.