Senior Statistical Programmer at Edetek

, , Poland -

Full Time

Start Date

Immediate

Expiry Date

13 Jun, 26

Salary

0.0

Posted On

15 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

SAS Programming, R Programming, Statistical Analysis, SDTM, ADaM, Tables, Listings, Figures, Data Manipulation, Programming Specifications, Regulatory Submissions, Clinical Trial Methodology, Data Validation, Problem-Solving, Communication

Industry

Software Development

Description

Edetek is seeking a highly skilled Senior Statistical Programmer to join our dynamic team. As a leader in data analytics, we are dedicated to providing innovative solutions to our clients in the pharmaceutical and healthcare sectors. In this pivotal role, you will leverage your expertise in statistical programming to ensure the integrity and quality of our data analyses. You will work closely with biostatisticians, clinical data managers, and other cross-functional teams to develop and execute statistical analyses that drive decision-making processes. The ideal candidate will have a strong background in programming languages such as SAS and R, as well as a deep understanding of clinical trial methodology and regulatory requirements. This position offers the opportunity to collaborate on high-impact projects, mentor junior programmers, and contribute to the development of our programming standards. If you are passionate about turning data into actionable insights and have a proven track record in advanced statistical programming, we invite you to apply and become a crucial part of our innovative team at Edetek. Responsibilities Develop and validate SAS programs to generate SDTM, ADaM datasets, tables, listings, and figures for clinical trial data. Collaborate with biostatisticians and data managers to understand project requirements and statistical analysis plans. Perform data manipulation and statistical analyses using appropriate programming techniques. Develop, review and critique programming specifications and outputs to ensure accuracy and compliance with standards. Mentor and provide guidance to junior statistical programmers to enhance their skills and productivity. Participate in the development and implementation of programming standards and best practices. Contribute to regulatory submissions by preparing documentation and providing support during audits. Bachelor's degree in Statistics, Biostatistics, Mathematics, or a related field; Master's degree preferred. Minimum of 5 years of experience in statistical programming within the pharmaceutical or clinical research industry. Proficiency in SAS programming; experience with R and other statistical software is a plus. Strong understanding of clinical trial design and regulatory requirements for statistical analysis. Experience with data management processes and data validation techniques. Excellent problem-solving skills and attention to detail. Strong communication skills, both verbal and written, to effectively collaborate with cross-functional teams. Benefits vary by country, but remain competitive. Below is a sample of the benefits offered to U.S. employees. Choice of comprehensive Medical, Vision and Dental Insurance plans Paid vacation time and sick days Corporate holidays annually Participation in the 401K Plan Comprehensive perks and discount programs for AAA, wholesale, insurance, Rx, fitness, pets, entertainment, etc. Health Advocate and Employee Assistance Program

Responsibilities

The Senior Statistical Programmer will develop and validate SAS programs to generate SDTM and ADaM datasets, tables, listings, and figures for clinical trial data. This role involves collaborating with biostatisticians and data managers to understand requirements and performing data manipulation and statistical analyses.