Argenta

Senior Clinical Trial Manager

Argenta

full-time

Posted on:

Location Type: Remote

Location: KansasUnited States

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Job Level

About the role

  • Obtains a clear understanding of all aspects of the study and defines roles of study personnel
  • Collaborates with the sponsor to establish projected study timelines for the study
  • Provides detailed oversight to ensure tasks are completed correctly and on time

Requirements

  • 8+ years clinical trial management experience within a Clinical Research Organization or major Animal Health pharmaceutical company
  • Proven experience in GCP late phase clinical trials
  • Animal health study protocol and final study report writing experience
  • Attention to detail and analytically driven
  • Dependability, flexibility and ability to multitask and manage time effectively
Benefits
  • Strong culture
  • Great benefits
  • Opportunity for growth
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical trial managementGCPstudy protocol writingstudy report writing
Soft Skills
attention to detailanalytical skillsdependabilityflexibilitymultitaskingtime management