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Thermo Fisher Scientific

via Workday

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Senior Programmer Analyst (Bioinformatics)

Anywhere
full-time
Posted 10/2/2025
Direct Apply
Key Skills:
SAS Programming
Data Set Structures
Complex Data Systems
Windows Office Applications
SAS Macro
Clinical Research
Quality Control Support
Project Management
FDA Standards
CDISC Standards
ADaM Standards
SDTM Standards
Data Analytics
Bioinformatics
Industrial Engineering
Computer Science

Compensation

Salary Range

$Not specified

Responsibilities

Independently create, execute, maintain and validate programs for data transfer and integration. Supervise and mentor other programmers while managing project timelines and ensuring high-quality deliverables.

Requirements

A Master's degree in a related field with three years of experience is required, or a Bachelor's degree with five years of experience. Candidates must have experience with SAS programming and clinical research.

Full Description

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Company Name: PPD Development, L.P. Position Title: Senior Programmer Analyst (Bioinformatics) Salary: $111,100.77 per year Location: 929 North Front Street, Wilmington, NC 28401 Summary of Duties: Independently create, execute, maintain and validate programs used to transfer data across multiple systems, integrate data from a variety of sources and structures, generate summary data from a variety of sources, generate reports or integrate multiple databases. Independently create, execute, maintain, publish and validate visualizations used in support of Risk Based and Centralized Monitoring. As a subject matter expert or Lead assist in creating tools, techniques and processes for automating Data Analytics tasks (Data integration automation, data retrieval automation, data mapping automation and automated report generation). Supervise and perform other programming tasks as necessary to support Data Analytics or other functional groups involved in Risk Based and Centralized Monitoring. Responsible for clearly documenting all work; managing assignments to meet timelines and delivering with high quality. Demonstrate a leadership level understanding of the role of the programmer in the overall process. Increase personal, peer and staff knowledge base and professional skills in areas including programming, risk-based monitoring, centralized monitoring, data science/data analytics, technology and techniques, clinical trials, and the pharmaceutical industry. Serve as a project lead; manage assignments to meet timelines and deliver high quality work, being familiar with any relevant contractual obligations or limits. Acts as mentor and first level escalation for Associate Programmer, Programmer Analyst I, Programmer Analyst II and Sr. Programmer Analyst. Supervise, train and mentor other programmers and CDLs. Work efficiently and effectively with little direct supervision. Participate in developing SOPs and working practice documents. Work with cross-functional project team leaders and client representatives to assess and develop project goals and timelines. Duties may be performed remotely. Qualifications: Master’s degree in Industrial Engineering, Bioinformatics, Data Analytics, Computer Science or a closely related field, and three (3) years of experience as a Statistical Programmer/Analyst or related role. In the alternative, the employer will accept a Bachelor’s degree in Industrial Engineering, Bioinformatics, Data Analytics, Computer Science or a closely related field, and five (5) years of experience as a Statistical Programmer/Analyst or related role. Must have three (3) years of experience with: SAS programming; Data set structures and working with complex data systems; Windows office applications; SAS Macro; and Clinical research and trials (Phases I, II, and III). Two (2) years of experience with: Quality control support. One (1) year of experience with: Project management; and FDA, CDISC, ADaM, and SDTM standards. Thank you for your interest as you consider starting a new career journey with us. As the world leader in serving science, our colleagues develop critical solutions through innovation—and build rewarding careers. Discover their extraordinary stories and connection to our Mission to enable our customers to make the world healthier, cleaner and safer. Their work is a story of purpose. What story will you tell? Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

This job posting was last updated on 10/3/2025

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