At BioBridges, we work with many exciting pioneers within the biopharmaceutical industry. These companies have a specific void in their internal resources and have asked BioBridges to find the right people to bridge that gap and span their Clinical Divide. The people we wish to work with are individuals who not only excel in their expertise and domain, but who also have high personal values and integrity to match. If that sounds like you, we would love to hear from you. All inquiries will be treated in the strictest confidence.

We are actively looking for consultants in the following areas:

Biostatistics

  • Biostatisticians
  • SAS Programmers
Clinical Data Management
  • Data Entry Operators
  • Clinical Data Managers
  • Clinical Data Programmers
  • Clinical Data Coders
  • CRO Oversight Managers
Clinical Monitoring Services
  • Regional CRAs and/or total Trial Teams
  • Inhouse Clinical Project/Study Managers
Clinical Quality & Compliance
  • Site Auditors
  • Vendor/CRO Auditors
  • In-house Auditors
Medical Writing
Medical Writers with experience writing:
  • Protocols
  • Investigator Brochures
  • Individual Clinical Study Reports
  • NDAs, BLAs, CTDs, 510k, PMAs, CMC Sections
Clinical Safety & Pharmacovigilance
  • Product Safety Specialists (pre and post market)
  • Safety MDs
Medical Information
  • Medical Information Specialists