Description
We are seeking a Senior Statistical Programmer (Sr SP) with 5-8 years of experience to join our Clinical Solutions team. The successful candidate will have end-to-end programming experience, strong hands-on expertise in SDTM, ADaM, and TLF development, exposure to efficacy endpoints and analyses, basic understanding or training in R Programming, and experience in Oncology.
Key Responsibilities:
- Develop custom programming code to generate summary tables, data listings, graphs, and derived datasets as specified in the statistical analysis plan and programming specifications.
- Ensure that outputs meet quality standards and project requirements, and perform validation programming.
- Maintain well-organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs.
- Manage scheduling and time constraints across multiple projects, set goals based on priorities from management, and adapt to timeline or priority changes.
- Prepare in advance for internal meetings, contribute ideas, and demonstrate respect for opinions of others.
- Conduct effective internal meetings, distribute relevant information, and ensure minutes are promptly and accurately distributed.
- Act as the lead statistical programmer, direct programming activities of other programming personnel, and monitor progress on programming deliverables.
- Participate in sponsor meetings, kickoff meetings, and bid defense meetings as statistical programming representative.
Requirements:
- Graduate degree, preferably in a scientific or statistical discipline.
- Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.
- Excellent written and verbal communication skills.
- Ability to read, write, speak, and understand English.