Consulting Opportunities

Advarra provides exciting and challenging consulting roles across a variety of life-sciences companies through our global consultant network. Our experts are experienced specialists with proven, successful experiences in clinical, quality, and regulatory specialty areas in the research and development (R&D) industry.

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Consulting

Auditing

Quality Auditors

Come grow with Advarra’s Quality Auditing Team! We are seeking additional Quality Auditors in Asia…

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In Demand Roles

The following roles are in high demand, and we welcome the opportunity to speak with you about your expertise in these areas.  Our Talent Management Department can be reached via email at AC_Resourcing@Advarra.com.

Advarra specializes in global GxP opportunities for Consultants with expertise in  Auditing,  Quality Management and Compliance, Risk Mitigation, and Inspection Readiness. These opportunities span across 6 continents and over 75 countries requiring fluency in various languages and Health Authorities. 

Advarra maintains an approved team of Quality Auditors ready to be assigned their next project.  These candidates have a minimum of 5 years’ experience,  excellent technical writing skills, and specific experience in a variety of the following areas:

  • GCP Audits (Site, Vendor)
  • GLP
  • GcLP
  • CSV
  • GVP
  • GMP
  • Fluency in any language
  • Health Authority knowledge (FDA, EMA, MHRA, PMDA, NMPA)

Advarra often has project opportunities for roles such as Directors of Clinical Operations, Clinical Research Coordinators, Regulatory Coordinators, Clinical Research Nurses, Project Managers, Data Specialists, or Study Activation Coordinators. 

Advarra has a high demand for experienced CRCs for our pharma and investigational site sponsors. We are seeking individuals with two to three years of experience with clinical trials, open to new opportunities for immediate discussion:

  • CRCs help sites support, facilitate, and coordinate daily clinical trial activities.
  • Collaborate and coordinate with the principal investigator (PI) on general study preparation and administrative duties.
  • Prepare and review protocols including the budget, informed consent, case report forms, regulatory binders, and other study documents.
  • Perform regulatory management of protocols, including preparation of safety reports, amendments/modifications, compliance renewals, and sponsor communications.
  • Manage the conduct of research by screening subjects for eligibility, registering participants, coordinating tests and procedures, collecting data, ensuring timely completion of case report forms, collecting, and submitting study documents to the sponsor, and generally working with the PI to manage the study’s day-to-day activities.
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