job summary:
- Experienced in ISS or ISE or integrating data across multiple clinical studies.
- In-depth understanding of CDISC Standards and creation of pooled data for integrated summary of safety analysis or for safety monitoring
- Experienced in leading statistical programming activities such as ADaM programming, Tables, listings, patient profiles, IB, DSUR, PSUR, Integrated Summary of Safety, Annual Safety Reports and/or other safety analysis.
- In-depth understanding of the drug development process, including experience with regulatory filings.
location: North Chicago, Illinois
job type: Contract
salary: $48 - 55 per hour
work hours: 8am to 4pm
education: Bachelors
responsibilities:
- Experienced in ISS or ISE or integrating data across multiple clinical studies.
- In-depth understanding of CDISC Standards and creation of pooled data for integrated summary of safety analysis or for safety monitoring
- Experienced in leading statistical programming activities such as ADaM programming, Tables, listings, patient profiles, IB, DSUR, PSUR, Integrated Summary of Safety, Annual Safety Reports and/or other safety analysis.
- In-depth understanding of the drug development process, including experience with regulatory filings.
qualifications:
- Experience level: Experienced
- Minimum 5 years of experience
- Education: Bachelors (required)
skills:
- PROGRAMMER ANALYST
- SAS
- data integration
- TLF Programming
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.