SP II
On-siteDurham, North Carolina, United States
Job Summary
Develop statistical programs for clinical trials, including data manipulation, table generation, and validation based on specifications. Ensure quality and integrity of analyses while representing the department in internal meetings. Collaborate with project teams to identify priorities, communicate timelines, and adapt to changing requirements. Complete work within known time and budget constraints while balancing multiple priorities. Maintain compliance with Good Clinical Practice and Standard Operating Procedures. This role supports statistical programming for tables, listings, and analysis datasets in accordance with PharPoint Research, Inc. policies. Occasional domestic or international travel may be required.
Required Qualifications
- Bachelor's degree (B.A./B.S.) or equivalent in Statistics, Computer Science or related field
- Knowledge of one or more statistical software packages used to conduct statistical analyses
- Ability to read, write, speak, and understand English
- Must have a valid driver's license with no limitations on driving availability
- Close vision and the ability to adjust focus
Desired Qualifications
- Experience in clinical research
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