Description
- Primary responsibilites include:
- Perform activities related to interim analysis and data base lock e.g data cleaning and clinical data review
- Assist in the implementation of tools for data review and cleaning
- Analyze and interpret study data and support preparation of reports for regulatory submissions.
- Review the SAE safety data to ensure data is accurately captured in the clinical database
- Must be fully knowledgeable and skilled in the development and writing of regulatory IND; NDA/sNDA; IB
- Work Experience:
- A minimum of 5+ years clinical development experience in the pharmaceutical or biotechnology industry is required; Oncology experience preferred
- Advanced Clinical/Science Degree (e.g. MD, PharmD, PhD, MSN, MPH)
To find out more about Real Staffing please visit www.realstaffing.com