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Clinical Affairs Staffing

Clinical Affairs Staffing Solutions​

Life Sciences companies around the world turn to TriNet Pharma to find professionals, including Clinical Trial Administrators, Clinical Research Associates and field-based monitors, with the expertise to coordinate projects or phases of the drug/device development process.

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We're Where You Need Us!

We’re not constrained by geographic location. Wherever in the world you need Clinical Affairs professionals, we’re there. Let us help you expand or build your organization.

Are you trying to fill critical Clinical Affairs roles?

TriNet Pharma can introduce you to Clinical Affairs professionals who are well-experienced in the areas of drug/device development, trial management, regulatory submissions and interactions, and post-approval product launch strategies.

Whether you have an overload of work or are designing a full-service
clinical program, our experienced and knowledgeable recruiters are ready to help you meet your program goals by:

  • Finding individuals for every level of organizational responsibility.
  • Locating and attracting individuals with the skills needed to meet your requirements.
  • Thoroughly vetting all candidates and only presenting you with those whose skills will help them succeed in a role.
  • Comprehensively managing all steps of the staffing process.

If you are under pressure to better manage Clinical Affairs functions, including staffing your teams more efficiently and effectively, and saving money while doing so, we can help!

TriNet Pharma has been in the business of Clinical Affairs
recruitment for life sciences companies since 2009, and we’re
uniquely positioned to help you optimize your team.

We can successfully complete executive search projects and help you fill assorted contract and direct-hire positions.

We can help you build a new Clinical Affairs team that can activate sites; build capacity in sites; identify key sites for clinical trials; engage with sites; data mining; quality data collection and analysis; risk management/mitigation; inspection readiness.
We can identify direct-hire professionals who will support the clinical development programs for an investigational lead drug candidate in company-sponsored and investigator-sponsored trials.
We can place contract professionals who can manage all aspects of multiple global clinical studies (Phase I through Phase IV).