At a Glance
- Tasks: Lead projects, write SAS/R programs, and ensure quality in clinical data processing.
- Company: Global Clinical Research Organisation with a focus on innovation and quality.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Join a dynamic team with global reach and excellent career advancement opportunities.
- Why this job: Make a real impact in the life sciences industry while developing your programming skills.
- Qualifications: Experience in statistical programming and a strong understanding of clinical research.
The predicted salary is between 60000 - 80000 £ per year.
Greetings! Tech Observer, a Global Clinical Research Organization (CRO) & FSP provider that has been supporting the Pharmaceuticals & Life Sciences Industry since 2005. We have offices in New Jersey, US (Headquarters), India, Denmark, UK & Singapore. Through our local partners, we extend our coverage to Australia, China, Malaysia, South Korea, Taiwan, Thailand, Vietnam, and other countries.
Job Responsibilities:
- Carry out all activities according to Tech Observer/Client SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).
- Ensure adherence to programming guidelines.
- Understanding of Protocol and SAP requirements.
- Lead the assigned project or task.
- Write SAS/R programs for development and QC of SDTM datasets, ADaM datasets and reports (i.e. Tables, Listings and Figures).
- Write SAS programs for development and QC of Randomization Schedule.
- Development and QC of SDTM and ADaM specifications.
- Development and QC of e-submission package for SDTM and ADaM.
- Review of study documents such as CRF, Metadata, Protocol, SAP and Mockshells.
- Demonstrate excellent problem-solving skills, a proactive approach and a willingness to take decisions on a regular basis.
- Perform function/project specific responsibilities as assigned.
- Demonstrate quick learning capabilities to improve programming and domain knowledge.
- Provide support in the driving system and process improvements, and to develop and implement solutions to improve efficiency and quality of clinical study data processing and reporting.
- Demonstrate 100% compliance and adherence to all SOPs.
- Prepare and implement standard operating procedures (SOP).
- Write complex SAS macros.
- Mentor junior statistical programmers and conduct knowledge sharing sessions.
Principal Statistical Programmer-FSP employer: Tech Observer
Tech Observer is an exceptional employer that prioritises employee growth and development within a collaborative and innovative work culture. With a strong commitment to quality and compliance, we offer our team members the opportunity to lead impactful projects in the dynamic field of clinical research, while enjoying the benefits of a global network and diverse work environment. Our focus on mentorship and continuous learning ensures that every employee can thrive and contribute meaningfully to the advancement of the Pharmaceuticals and Life Sciences industry.
