Job Description
Clinical Research Data Coordinator – Oncology
Onsite Contract
Required Qualifications
+ MUST HAVE 3 years of clinical research data coordination experience
+ MUST HAVE oncology clinical research experience including Phase I, II, or III studies
+ MUST HAVE experience with:
+ Clinical trial data entry and management
+ Query resolution
+ Electronic Data Capture (EDC) systems
+ Electronic Medical Records (EMR)
+ Clinical research documentation and compliance
+ Experience working with sponsors, CROs, and monitoring teams
+ Strong attention to detail and organizational skills.
+ Excellent written and verbal communication skills.
+ Ability to work independently while managing multiple studies and competing priorities.
+ Bachelor's degree in a scientific, healthcare, or related field
Responsibilities
Data Management
+ Abstract and collect ...
Onsite Contract
Required Qualifications
+ MUST HAVE 3 years of clinical research data coordination experience
+ MUST HAVE oncology clinical research experience including Phase I, II, or III studies
+ MUST HAVE experience with:
+ Clinical trial data entry and management
+ Query resolution
+ Electronic Data Capture (EDC) systems
+ Electronic Medical Records (EMR)
+ Clinical research documentation and compliance
+ Experience working with sponsors, CROs, and monitoring teams
+ Strong attention to detail and organizational skills.
+ Excellent written and verbal communication skills.
+ Ability to work independently while managing multiple studies and competing priorities.
+ Bachelor's degree in a scientific, healthcare, or related field
Responsibilities
Data Management
+ Abstract and collect ...