Work alongside experienced pharmacovigilance resources to support clinical trial and post-marketing safety surveillance throughout the clinical trial and post-marketing/commercialization phases of your product lifecycle.
Our resources can be utilized to meet the wide range of drug safety and pharmacovigilance requirements throughout the life sciences, as well as to support staffing assignments, lead and manage related activities, bridge staffing gaps, and provide long-term or interim leadership.
Please contact us to learn more about fulfilling specific pharmacovigilance resourcing needs. We help clients secure a wide variety of drug safety resources for both contracted and direct hire engagements with the perfect combination of qualifications, experience, and motivation for succeeding in challenging and demanding projects.
Get quick, easy access to industry resources.
Fulfill short or long-term resourcing needs at a competitive rate.
Get a flexible alternative to traditional full-time hiring.
Receive dedicated project management and a Total Quality Guarantee.
Read our brochure to learn more about our full range of life science resourcing capabilities.