Senior Programme Associate Job at Agrotec Spa

Senior Programme Manager - Public Sector Engagement

The purpose of this role is to lead engagement for techUK’s Public Services Boar...

Location

United Kingdom , London

Salary:

40000.00 - 45000.00 GBP / Year

techUK

Expiration Date

Until further notice

Requirements

Strong interest in innovation, the use of technology in the public sector and the UK tech industry
Good connections with a network of with senior public sector stakeholders
A self-motivated individual with a positive can-do approach who is comfortable working with competing demands and responding to tight deadlines
Good organisational skills and attention to detail
Excellent written and verbal communication skills with the ability to communicate technical and policy information effectively to a range of audiences
A team player who has experience of managing relationships with a diverse range of stakeholders and is comfortable working with senior individuals in industry
Comfortable with public speaking
Demonstrates an understanding of the Government procurement landscape and the positioning and role of trade bodies
Good high-level knowledge of technology and workings of the technology sector
Demonstrates a strong understanding of the public sector tech market

Job Responsibility

Lead senior level public sector stakeholder engagement for techUK’s Public Services Board, ensuring monthly access to high-level decision makers in government
Liaise with the Chair and Vice Chair of PSB to support the smooth running of the monthly meeting
Support the development, commissioning and publication of at least one PSB report per year
Organise 2 PSB stakeholder dinners a year and a unique member excursion for learning and development purposes
Coordinate activities with other public sector facing member-led committees, and plan at least one cross programme activity
Raise the public profile of the PSB through media engagement and public facing events
Liaise with other techUK teams to identify and exploit cross-fertilisation opportunities with other programmes within techUK
Deputise for the Associate Director, Central Government and Education in their absence as requested
and Any other duties that might from time to time be required by the Associate Director, Central Government and Education and the techUK leadership team.

What we offer

discretionary bonus and comprehensive benefits

Fulltime

Applications Development Senior Programmer Analyst

Citibank, N.A. seeks an Applications Development Senior Programmer Analyst for i...

Location

United States , Tampa, Florida

Salary:

Not provided

Citi

Expiration Date

Until further notice

Requirements

Master’s degree, or foreign equivalent, in Computer Science, Computer Engineering, or related field and 3 years of progressive, post-baccalaureate experience as a Software Engineer, Full-Stack Java Developer, or related position involving frontend and backend full software development lifecycle including post-implementation user support
Alternatively, will accept a Bachelor’s degree in the stated field and 5 years of the specified progressive, post-baccalaureate experience
Java for backend code writing and maintenance of web services
Angular for frontend development
TypeScript to write TypeScript code for Angular application
SQL server, MySQL, Oracle for database design and management
Backend development using Spring
RESTful API building
Jira
Confluence

Job Responsibility

Monitor and control all phases of the applications development process including analysis, design, construction, testing, implementation, and user supports
Analyze the complex business processes, systems and industry standards associated with Citi Flexcube and Cash to provide the necessary solutions for Global Finance Customer Identification, specifically with the internal process of accounts opening, Auto Investment and Statement
Acts as SME to senior stakeholders and /or other team members
Adhere to the defined internal process of application development, and use JIRA for requirements and tasks controls and Bitbucket for version control
Develop and generate the reports requested based on business needs using Cognos Analytics
Configure and manage build pipelines for continuous integration and continuous deployment using TeamCity
Create deployment plans and workflows to automate application deployments across different environments using UDeploy
Execute production releases following the internal process, create a runbook of the steps in Confluence page, and manage change requests release using Service Now
Monitor AutoSys jobs and use Confluence pages to document project plans, requirements, meeting notes, and other important information
Develop reusable Angular components in accordance with the Citi standard

What we offer

medical, dental & vision coverage
401(k)
life, accident, and disability insurance
wellness programs
planned time off (vacation)
unplanned time off (sick leave)
paid holidays

Fulltime

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle and excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards with strong ability to implement the standards
In depth knowledge of SAS/STAT packages
Familiar with data quality and compliance check tools

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
At least 4 years of statistical programming experience in a clinical development environment
Familiarity with drug development life cycle
Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards
Familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Job Responsibility

Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

Senior Programme Associate

Agrotec Spa

Location:

Category:
-

Contract Type:
Not provided

Salary:

Requirements:

Additional Information:

Job Posted:
January 19, 2026

Expiration:
January 25, 2026

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Agrotec Spa

Location:

Category:-

Contract Type:Not provided

Salary:

Requirements:

Additional Information:

Job Posted:January 19, 2026

Expiration:January 25, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

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Category:
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Contract Type:
Not provided

Job Posted:
January 19, 2026

Expiration:
January 25, 2026