Data Coordinator
About the role
The Data Coordinator provides support to the Clinical Research Coordinator (CRC) and Research Nurse on a daily basis, ensuring all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines.
Responsibilities
- Supports the CRC to meet industry trial data deadlines
- Obtains source documentation for patients enrolled onto clinical trials
- Aids in case report form completion and query resolution
- Aids in Serious Adverse Event (SAE) reporting and tracking
- Creates and maintains patient visit tracking spreadsheets for CTS
- Maintains and archives study administrative files
- Maintains and archives regulatory files
- Assigns special procedural projects to enhance the functioning of the research program
- Affirms adherence to SCRI SOPs, Good Clinical Practice (GCP) and ICH regulations and guidelines throughout the clinical trial conduct
Requirements
- Knowledge of scientific, medical, and regulatory terms
- Knowledge of GCP and Good Manufacturing Practice (GMP)
- Detail-oriented
- Excellent English written and oral skills
Qualifications
- Bachelor Degree preferred
- Healthcare experience, Clinical trials support, or pharmaceutical industry experience preferred
Skills
- Strong organizational skills
- Attention to detail
- Ability to manage multiple tasks simultaneously
- Excellent communication skills
Pay
The compensation range for this position is $24/hr - $27/hr.
Schedule
Full-time
Benefits
We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That's why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here.