Current jobs related to Statistical Programmer - United Kingdom - Tech Observer

  • Statistical Programmer

    1 day ago

    United Kingdom Worldwide Clinical Trials Full time

    External Description: Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical...

  • Statistical Programmer

    4 weeks ago

    United Kingdom Worldwide Clinical Trials Full time

    External Description:Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials,...

  • Statistical Programmer

    1 week ago

    United Kingdom Worldwide Clinical Trials Full time

    External Description:Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials,...

  • Principal Statistical Programmer

    4 weeks ago

    United Kingdom Warman O'Brien Full time

    Principal Statistical Programmer | Leading CRO | Home Based | UK | Europe | Permanent |Award winning global CRO is seeking an experienced Principal Statistical Programmer to join their expanding team. In this client-facing position, you will oversee 1-2 complex projects, prioritizing the development of long-term client relationships. Your responsibilities...

  • Senior Statistical Programmer

    1 day ago

    United Kingdom EPHARMIT LIMITED Full time

    Our client is a global pharmaceutical brand who are expanding their programming and statistical teams. They are currently looking for senior level (and above) programmers who will be engaged on inital 12 month contracts on a fully remote basis. Programming is the department that oversees and delivers the programming aspects of clinical drug development,...

  • Senior Statistical Programmer

    3 weeks ago

    United Kingdom EPHARMIT LIMITED Full time

    Our client is a global pharmaceutical brand who are expanding their programming and statistical teams. They are currently looking for senior level (and above) programmers who will be engaged on inital 12 month contracts on a fully remote basis.Programming is the department that oversees and delivers the programming aspects of clinical drug development,...

  • Senior Statistical Programmer

    1 week ago

    United Kingdom EPHARMIT LIMITED Full time

    Our client is a global pharmaceutical brand who are expanding their programming and statistical teams. They are currently looking for senior level (and above) programmers who will be engaged on inital 12 month contracts on a fully remote basis.Programming is the department that oversees and delivers the programming aspects of clinical drug development,...

  • Data Analysis Programmer

    1 day ago

    United Kingdom Worldwide Clinical Trials Full time

    It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of almost 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. What Global Programming does...

  • Statistical Programming Training Coordinator

    1 day ago

    United Kingdom Veramed Full time

    Join Our Team as a Statistical Programming Trainer - R Language! We are excited to invite an experienced Statistical Programming Trainer to develop and implement R language training programs for our permanent SAS programming workforce. This unique role offers the opportunity to make a significant impact within our organization and help shape the future of...

  • Statistical Programming Training Coordinator

    3 weeks ago

    United Kingdom Veramed Full time

    Join Our Team as a Statistical Programming Trainer - R Language!We are excited to invite an experienced Statistical Programming Trainer to develop and implement R language training programs for our permanent SAS programming workforce. This unique role offers the opportunity to make a significant impact within our organization and help shape the future of...

  • Statistical Programming Training Coordinator

    1 week ago

    United Kingdom Veramed Full time

    Join Our Team as a Statistical Programming Trainer - R Language!We are excited to invite an experienced Statistical Programming Trainer to develop and implement R language training programs for our permanent SAS programming workforce. This unique role offers the opportunity to make a significant impact within our organization and help shape the future of...

  • Training/Programme Manager

    1 day ago

    United Kingdom Veramed Full time

    Join Our Team as a Statistical Programming Trainer - R Language! We are excited to invite an experienced Statistical Programming Trainer to develop and implement R language training programs for our permanent SAS programming workforce. This unique role offers the opportunity to make a significant impact within our organization and help shape the future of...

  • Senior SAS Programmer

    1 day ago

    United Kingdom Warman O'Brien Full time

    Senior Statistical Programmer – FSP | Global CRO | Fully Remote | UK | Europe | In this role, you will lead programming activities for complex clinical studies, manage resources, allocate tasks, and track progress to meet project timelines and quality standards. Lead programming for multiple complex studies. 5+ years of experience in statistical...

  • Principal SAS Programmer

    1 month ago

    United Kingdom Evidencia Scientific Search and Selection Limited Full time

    Principal (Senior Programmer and Project Manager) Real World Evidence & Data Analytics* US or UK based A great opportunity to join an international healthcare consultancy providing value evidence strategy, generation, synthesis, and communication services to life sciences companies. Delivering these services empowered by technology innovations has enabled...

  • Contract Senior SAS Programmer

    2 weeks ago

    United Kingdom MAC Clinical Research Full time

    supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area; reviewing Statistical Analysis Plans (SAPs), including study specific ISS/ISE and DSMB SAPs and...

  • Contract Senior SAS Programmer

    2 weeks ago

    United Kingdom MAC Clinical Research Full time

    supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area; reviewing Statistical Analysis Plans (SAPs), including study specific ISS/ISE and DSMB SAPs and...

  • Senior SAS Programmer

    7 days ago

    United Kingdom MAC Clinical Research Full time

    We are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

  • Senior SAS Programmer

    2 weeks ago

    United Kingdom MAC Clinical Research Full time

    We are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

  • Senior SAS Programmer

    2 weeks ago

    United Kingdom MAC Clinical Research Full time

    We are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

  • Senior SAS Programmer

    2 weeks ago

    United Kingdom MAC Clinical Research Full time

    We are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

Statistical Programmer

2 months ago

United Kingdom Tech Observer Full time

Tech Observer is a Global CRO with HO in NJ, USA and presence in other 20+ countries-India, Denmark, UK, Singapore etc. (www.tech-observer.com)


We are hiring for following roles Statistical programmers for FSP (US timing)


Location-United Kingdom (candidates eligible to work in UK shall be considered)


Job Responsibilities-


1.Compliance with working SOPs within the framework of the Quality Management System and to Good Clinical Practice (GCP). Ensure adherence to programming guidelines.

2. Implement and follow the latest versions of CDISC, FDA Guidelines, GCP and other industry standards.

3. Participate in and co-ordinate the Statistical Programming review of Case Report Forms (CRFs), annotated CRFs, database structures and study related documentation (e.g. data validation guidelines).

4. Review and interpret Report and Analysis Plans and provide comments for assigned projects.

5. Develop and review SAS programs and output for the management of clinical trial data, the tabulation of data, preparation of patient data listings, graphical output, and creation of derived datasets and statistical analysis of data as specified in the Statistical or Report Analysis Plans.

6. Develop SAS programs for ad hoc tables and listings. Write, modify, and maintain programs that produce diagnostics and listing for data review in support of Data Management

7. Carry out electronic data transfer (both incoming and outgoing). Develop and review programs to ensure the data transfer has been produced to specification.

8. Design and set-up utilities/SAS based systems to assist and facilitate Clinical Data Management activities.

9. Review draft and final production runs for projects to ensure quality and consistency.

10. Provide feedback for continuous improvement of SOPs from BPP and other cross functional SOPs.

11. Ensure quality of personal work and the work of the team when acting as a Lead Programmer or Biometrics Project Manager.

12. Assume team member responsibilities, including representing Statistical Programming at internal project team meetings, client meetings and audits.

13. With sufficient experience may support the activities of senior Statistical Programming staff by providing input into time and cost estimates and presentations to clients.

14. Advise Senior Statistical Programming staff of changes in scope of projects to enable the timely development of change orders.

Demonstrate excellent problem solving skills, a proactive approach and a willingness to take decisions on a regular basis.

16. Encourage and participate in the ongoing review of the processes used by the Statistical Programming group to ensure processes are continually improved.

17. Maintain awareness of new developments in programming techniques and IT which may be applied to the management and reporting of clinical trial data.

18. Perform other duties as assigned by senior Statistical Programming staff.