Associate Scientist Job at Certara UK
Step into one of the most promising Scientist jobs in the UK with Certara, a global leader in biosimulation and advanced drug development analytics. This Associate Scientist, SAS Programmer position is a powerful opportunity for professionals seeking a high-impact life science career, especially Jobs for Life Science Graduates eager to enter a world-class scientific environment. Ideal for analytical and innovation-driven minds, this role positions you at the forefront of clinical data science and regulatory insight.
About the Company
Certara is a global biosimulation and drug development leader, offering advanced software, analytics, and consulting solutions used by biopharma, academia, and regulatory authorities worldwide. As the world’s largest Clinical Pharmacology and Pharmacometric organization, Certara empowers scientists to accelerate safer, more effective medicines. With a mission to transform drug development, Certara provides a thriving environment for professionals pursuing meaningful Scientist jobs and long-term life science career growth.
Job Details:
- Job Title: Associate Scientist, SAS Programmer
- Location: United Kingdom
- Category: Scientific
- Job ID: 2305
Scientist Job Overview
Certara accelerates medicines using proprietary biosimulation software, technology, and services that transform traditional drug discovery and development. With more than 2,000 clients across 62 countries—including biopharmaceutical companies, academic institutions, and regulatory agencies—Certara is the world’s largest Clinical Pharmacology & Pharmacometrics organization.
As part of this division, you will contribute to integrating advanced simulation approaches into critical drug development deliverables, informing decision-making and strengthening global regulatory submissions.
Responsibilities
- Manage and prepare CDISC ADaM/SDTM datasets (e.g., ADPC, PP, ADPP) for advanced analyses such as PopPK and PK/PD modeling.
- Interface directly with clients regarding data transfers, dataset specifications, and data queries.
- Create electronic submission packages for regulatory agencies.
- Conduct QC/QA on datasets and reports.
- Participate in initiatives to improve efficiency in data management, analysis, reporting, and automation.
- Collaborate with associates, expert modelers, and drug development consultants across a wide range of therapeutic areas and data types.
Qualifications For a Scientist Job
- BS/MS (or equivalent) in Life Sciences, Bioinformatics, or a related field.
- 1–5 years of experience in data management, data analysis, report writing, and regulatory drug submissions.
- Advanced proficiency in SAS (SAS9-Base); experience with R is a plus.
- Familiarity with CDISC data formats.
- General understanding of clinical drug development, pharmacokinetics, and pharmacology.
- Strong accuracy, attention to detail, and ability to deliver work on time.
- Ability to manage multiple collaborative projects; strong team-oriented mindset.
- Excellent written and verbal communication skills in English.
- Motivated, eager to learn, and committed to growth and development.
