Our consultants can provide coverage through every phase of our clients’ clinical trials, with top talent at all career levels and a wide range of specialties, including, but not limited to:

  • Biometrics
    • Biostatistics
    • Statistical programming (SAS)
    • Clinical data management
      • Project management & vendor oversight, clinical database programming (EDC)
    • Data standardization
      • CDISC (SDTM, ADaM, TLG, define.xml), CDASH (TAUG)
  • Medical Writing
    • Regulatory and submission level documents
      • IND/IDE, NDA, ANDA, PMA, BLA, 510(k), RPS, eCTD
    • Clinical protocols, Clinical Study Reports (CSR), Clinical Evaluation Reports (CER)
    • Briefing documents, Investigator Brochures (IB), Informed Consent Forms (ICF)
    • Publications, manuscripts, journals, literature reviews, poster presentations
  • Clinical Operations
    • Monitoring
    • Clinical trial design, protocol development, and full lifecycle study management
    • Project management, clinical trial management, and vendor oversight
  • Medical Affairs and Regulatory Affairs
    • Pharmacovigilance/drug safety
    • Medical monitoring
    • Quality assurance auditing

We have consultants on assignment throughout the U.S. and Europe. Trust Oxford Life Sciences to provide you with unparalleled recruiting and consulting services, and see why the majority of our clients would recommend our services to others.

Download our datasheet, find out if your needs match our services, or give us a call at (800) 426-9196.