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Seeking a full-time, Pharm-B REGULATORY EXPERIENCE, office-based Clinical Trial Coordinator to join our Data Management team.

This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

Track case report forms

Clean the clinical database, which includes generating and resolving data clarifications

Update the clinical database
Reconcile clinical data Maintain study documentation

Perform QC audits of the clinical database

QUALIFICATIONS

Bachelor’s degree in a health-related field with strong attention to detail and working knowledge of Excel and Word

Experience – 1-2 years of experience working at a site as a Clinical Trial Coordinator is REQUIRED
Job Type: Full-time

Application process – interested Cand6 Kindly Send Your Resume’s to joe@kalkonclinical.com

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