At a Glance
- Tasks: Lead projects, write SAS/R programs, and ensure quality in clinical data processing.
- Company: Global Clinical Research Organisation with a strong presence in the Pharmaceuticals & Life Sciences industry.
- Benefits: Competitive salary, flexible working 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 healthcare by improving clinical study data quality.
- Qualifications: Experience in SAS programming and a solid understanding of clinical research.
The predicted salary is between 60000 - 80000 £ per year.
Tech Observer, a Global Clinical Research Organization (CRO) & FSP provider, 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 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 SAS Programmer employer: Tech Observer
At Tech Observer, we pride ourselves on being an exceptional employer in the clinical research field, offering a collaborative and innovative work culture that empowers our employees to excel. With a strong focus on professional development, we provide ample opportunities for growth and mentorship, particularly for roles like the Principal SAS Programmer, ensuring that our team members are equipped with the skills needed to thrive in a dynamic environment. Located in New Jersey, our headquarters fosters a supportive atmosphere where creativity and problem-solving are encouraged, making it an ideal place for those seeking meaningful and rewarding careers in the Pharmaceuticals and Life Sciences industry.
