Statistical Programming Consultant
W2 Contract
Salary Range: $166,400 - $176,800 per year
Location: Redwood City, CA - Hybrid or Remote PST
Job Summary:
In this role, you will be responsible for statistical programming and verifying clinical trial data to produce high-quality deliverables in a fast-paced environment. You will need to consistently meet study timelines, quality standards, and requirements and be required to work closely and communicate effectively with internal team members, statisticians, and other functional group members to complete deliverables.
Duties and Responsibilities:
- Provide Statistical Programming support in either production or verification of SAS scripts and outputs for Analysis Files, Tables, Listings, Figures, and any other form of Clinical Trial Data, in addition to writing analysis file specifications and other relevant documentation of deliverables and analysis methods.
- Ensure effective planning to meet quality and timely delivery of deliverables.
- Comply with project and study programming standards and specifications following internal guidelines.
- Ensure the accuracy of clinical trial results for internal and external audiences (e.g., regulatory authorities, academic community, and healthcare providers) via biometrics QC of documents with clinical data.
- Provide programming support for relevant deliverables, such as Investigator Brochures, publications, and US and ex-US regulatory submissions, including CDISC-compliant datasets (SDTM, ADaM) and data documentation, Reviewer's Guide, TLFs, Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response).
- Perform hands-on programming of in-house deliverables, including Dose Committee meetings, Board of Director meetings, and Exploratory Analysis.
- Verify and review Statistical Analysis Plans (SAP), documents, spreadsheets, and slides for in-house presentations and external publications.
Requirements and Qualifications:
- MS, BS/BA degree, or other suitable qualifications relevant to the field.
- 6-8+ years of statistical programming industry experience with clinical trial data using SAS software
- Proficiency in SAS Studio or PC SAS
- A fast learner with a demonstrable record of teamwork
- Thrives in a collaborative team setting and is driven by a desire to deploy and adopt innovative approaches and technologies in a high-energy environment.
- Excellent written and verbal communication skills
- Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute goals as a member of an interdisciplinary team
- Oncology experience is preferred.
Desired Skills and Experience
Statistical programming, clinical trial, SAS Studio, PC SAS, Oncology
Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate.
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