Associate Programmer Analyst – Clinical Research & SAS

Work Schedule

Environmental Conditions

Job Description

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 countries in the last 5 years.

As part of our expert team youll have the opportunity to ensure operational excellence that makes a real difference in clinical trials.

As an Associate Programmer Analyst you will provide bioinformatics programming support for some or all of the following activities: creation and maintenance of programs used for data management data validation analysis data statistical report generation and program validation.

You will communicate effectively within a multidisciplinary project team to complete assigned tasks on time and within budget.

• Performs programming support tasks as assigned by study/project team leads that includes but is not limited to creating executing maintaining and validating programs that transfer data across multiple data management systems or operating systems combining data from a variety of sources and structures generating and storing summary data from a variety of sources generating reports or combining multiple databases and validating programs that generate listings tables and figures using SAS and standard tools and processes.
• Actively seeks information to gain a good understanding of the programming role and the overall process including following departmental working practice documents and SOPs.
• Documents all work and manages own assignments to meet timelines and deliver high quality.
• Functions as a team member by working with study team leads to ensure they are kept informed of progress on tasks assigned.
• Increases knowledge base and professional skills in areas including programming technology and techniques clinical trials and the pharmaceutical industry by working closely with mentors attending presentations teaching events and contributing to other general department documents and policies by assisting mentors with implementing best practice documents and articles.

• Bachelors degree in computer science statistics biostatistics mathematics or related field or equivalent and relevant formal academic/vocational qualification.
• Previous experience that provides the knowledge skills and abilities to perform the job comparable to 0 to 2 years.
• In some cases an equivalency consisting of a combination of appropriate education training and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.

• Fundamental understanding of one or more programming languages.
• Essential attention to detail.
• Decent problem solving skills.
• Decent written and verbal communications skills.
• Basic organizational skills with the ability to adapt and adjust to changing priorities.
• Positive attitude and the ability to work well with others.
• Demonstrated initiative and motivation.

Work is performed in an office environment with exposure to electrical office equipment.

Occasional drives to site locations with occasional travel both domestic and international.

When you join Thermo Fisher Scientific you become part of a global team that values passion innovation and a commitment to scientific excellence.

Youll work in an environment where collaboration and development are part of the everyday experienceand where your contributions truly make a difference.

Apply today to help us deliver tomorrows breakthroughs.