Bioanalytical Study Manager

PPD (Thermo Fisher)

Remote
Fully remote
Bioanalytical operations for pre-clinical studies
Vendor management for lab service providers
Study coordination and sample analysis
Thermo Fisher is seeking a Bioanalytical Study Manager for a fully remote position that supports client studies in the pharmaceutical and biopharmaceutical sectors. The role involves managing bioanalytical operations for pre-clinical studies and clinical trials, requiring strong project management and communication skills, as well as experience in bioanalytical laboratory settings

Job Summary

  • Manage bioanalytical operations for pre-clinical studies and clinical trials, ensuring timely delivery of quality data by coordinating activities between multiple stakeholders.
  • Support the team contracting with third-party lab service providers for assay development and validation.
  • Join our dynamic team and lead the charge in supporting our clients development pipeline from a bioanalytical perspective.

Matching Summary

Match Score: 85

Thermo Fisher is seeking a Bioanalytical Study Manager for a fully remote position that supports client studies in the pharmaceutical and biopharmaceutical sectors. The role involves managing bioanalytical operations for pre-clinical studies and clinical trials, requiring strong project management and communication skills, as well as experience in bioanalytical laboratory settings.

Skills & Requirements

Must-have

  • Bioanalytical operations for pre-clinical studies
  • Vendor management for lab service providers
  • Study coordination and sample analysis
  • Input into clinical trial documents
  • Experience performing PK/ADA assays
  • Large molecule immunoassay-based bioanalysis

Nice-to-have

  • Translational or biomarker experience
  • Biomarker techniques and flow cytometry
  • Multicolor panel design and gating strategy
  • Data analysis in FlowJo

Key Requirements

  • BA/BS in a scientific degree + 2 years’ experience in a Bioanalytical laboratory
  • Experience in a regulated environment
  • Understanding of clinical trial design
  • Good project management background
  • Legally authorized to work in the United States without sponsorship

Work Rights

Must be legally authorized to work in the United States

Tailored Resume

Cover Letter