As a Principal Programmer Analyst, you will lead the development and execution of programming strategies for clinical trials, ensuring data integrity and accuracy. Responsibilities include collaborating with teams, mentoring junior programmers, and implementing innovative programming techniques.
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Contribute to world-class scientific research as a Senior Trial Programmer at Thermo Fisher Scientific Inc., where you will develop and implement flawless programming solutions.Key Responsibilities
- Lead the development and execution of programming strategies for clinical trials.
- Collaborate with cross-functional teams to determine the most effective programming solutions.
- Ensure the integrity and accuracy of trial data through rigorous validation processes.
- Successfully implement innovative programming techniques to streamline trial processes.
- Provide mentorship and guidance to junior programmers, encouraging a culture of continuous improvement and excellence.
- Stay up-to-date with industry trends and technological advancements to maintain our competitive edge.
Requirements
- Proven experience as a trial programmer in the information technology sector.
- Outstanding focus on detail and dedication to delivering high-quality results.
- Ability to strictly adhere to regulatory guidelines and industry standards.
- Demonstrated ability to collaborate with diverse teams and drive projects to successful completion.
- Excellent problem-solving skills and the ability to adapt to evolving project requirements.
- A degree in Computer Science, Information Technology, or a related field or equivalent experience is preferred.
Join our team and be a part of an organization that values your expertise and contributions. At Thermo Fisher Scientific Inc., we are committed to crafting a work environment where you can thrive and make a significant impact.
Top Skills
Clinical Trials
Industry Standards
Programming Solutions
Programming Strategies
Regulatory Guidelines
Validation Processes
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