A leading oncology research company located in Phoenix is seeking a Clinical Data Coordinator I to manage clinical data entry activities for various medical affairs protocols. This role involves ensuring data integrity, reviewing clinical protocol research data, and performing quality audits on databases within compliance guidelines. The ideal candidate will have 3-5 years of experience in clinical research settings, particularly in oncology, and possess strong data collection and communication skills. The position may require travel to multiple sites.
Qualifications
3-5 years of experience in a GCP/clinical research regulatory environment.
Strong medical terminology understanding.
Experience in training and mentoring less experienced colleagues.
Responsibilities
Abstract clinical data from subject source documentation.
Enter clinical data into study specific EDC case report forms.
Perform QC audits of the clinical database.
Skills
Data collection activities
Oncology clinical studies
Communication skills
GCP knowledge
EDC systems experience
Microsoft Office Suite proficiency
Tools
EDC systems
Microsoft Excel
Microsoft Word
Job description
A leading oncology research company located in Phoenix is seeking a Clinical Data Coordinator I to manage clinical data entry activities for various medical affairs protocols. This role involves ensuring data integrity, reviewing clinical protocol research data, and performing quality audits on databases within compliance guidelines. The ideal candidate will have 3-5 years of experience in clinical research settings, particularly in oncology, and possess strong data collection and communication skills. The position may require travel to multiple sites.