Senior Associate Operational Excellence & Compliance

Integrated Resources, Inc

  • Cambridge, Massachusetts
  • 6 days ago
  • Contractor
Want to know if you’re a fit?
Upload your resume and let our AI show you.

Skills

  • Auditingunmatched
  • Change Controlunmatched
  • Clinical Researchunmatched
  • Communication Skillsunmatched
  • Corrective Actionunmatched
  • Detail Orientedunmatched
  • FDA (Food and Drug Administration)unmatched
  • File Systemsunmatched
  • GCP (Good Clinical Practices)unmatched
  • ICH Regulationsunmatched
  • Information Technology & Information Systemsunmatched
  • Internal Auditunmatched
  • Interpersonal Skillsunmatched
  • Metricsunmatched
  • Operations Researchunmatched
  • Pharmacovigilanceunmatched
  • Presentation/Verbal Skillsunmatched
  • Process Analysisunmatched
  • Process Developmentunmatched
  • Process Improvementunmatched
  • Regulationsunmatched
  • Regulatory Requirementsunmatched
  • Rehabilitation Nursingunmatched
  • Reporting Skillsunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Writing Skillsunmatched

Description

Senior Associate Operational Excellence & ComplianceA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionPrincipal DutiesCollaborates with internal departments on implementation of quality principles and regulatory requirements related to Good Pharmacovigilance Practice (GVP)Coordinates PV-related aspects of inspection readiness activitiesAssists and other departments in addressing audit findings and development of Corrective and Preventative Actions (CAPAs)Participates in development and reporting of compliance metrics related to GVP activitiesConducts effectiveness checks and internal assessments of current processes and procedures to identify potential process improvement opportunitiesAssist in hosting of regulatory inspections related to PVApplies departmental SOPs and participates in the development of departmental SOPs, as appropriateResponsible for maintenance, update, and change control of the Pharmacovigilance System Master File (PSMF)Monitors commitments from internal audit and regulatory inspection findingsPerforms late case investigations and writes delayed case reportsQualificationsQualifications and Experience:In depth understanding of clinical research and pharmacovigilance operations and regulations-in particular an excellent knowledge of ICH GCP, GVP as well as FDA, EU and ROW regulations5 + years of experience in clinical research and/or pharmacovigilance, including complianceTeam player with excellent interpersonal skillsStrong attention to detail and excellent communication skills, both written and oral.Excellent knowledge of SOPs and auditing/compliance background preferredEducation:Bachelor's Degree required.Master's Degree preferred.

Numbers & Facts

LocationCambridge, Massachusetts
Job TypeContractor

Similar Jobs

See more jobs