Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Manage and prepare data sets for drug development analysis and create submission packages.
- Company: Join Certara, a leader in biosimulation software transforming drug discovery globally.
- Benefits: Enjoy a collaborative work environment with opportunities for personal growth and career pathways.
- Why this job: Be part of impactful projects that shape the future of medicine and enhance your skills.
- Qualifications: BSc/MSc in relevant fields with SAS expertise and experience in data management required.
- Other info: Diversity and merit-based hiring ensure a welcoming workplace for all.
The predicted salary is between 36000 - 60000 £ per year.
Overview
Certara accelerates medicines using proprietary biosimulation software, technology, and services to transform traditional drug discovery and development. Its clients include more than 2,000 biopharmaceutical companies, academic institutions, and regulatory agencies across 62 countries.
We are the largest Clinical Pharmacology & Pharmacometric organization in the world, which enables us to assure that various career pathways are offered which match the ambition and personal interests of our employees! As one of Certara’s divisions, we deliver value by integrating advanced simulation approaches into the most crucial drug development deliverables – to inform internal decision-making and strengthen global regulatory submissions. Leveraging our experience in working on thousands of drug development projects on behalf of hundreds of biopharma companies, we bring a track record of success and a broad range of expertise to each assignment.
Responsibilities
As data programmer you manage and prepare CDISC ADaM/SDTM data sets (ADPC, PP and ADPP) and data for state-of-the-art analysis, such as PopPK or drug exposure-response (PKPD). You interact directly with the client on topics around data transfers, dataset specifications and data queries. Following completion of the project deliverables, you will create an electronic submission package for future submission to regulatory agencies. In addition, you will conduct quality control and quality assurance activities on datasets and reports and may participate in company initiatives to improve efficiency of data management, analysis and reporting (IT, methodology, automation, quality).
As data programmer you will work closely in teams with other associates, (experts) modelers and drug development consultants supporting a wide variety of client projects (therapeutic areas, data types).
Qualifications
- BSc, MSc or equivalent in Pharmaceutical- or Life Sciences, Statistics/Mathematics/Bio-Informatics, or related fields with 1- 5 years’ experience in data management and analysis, report writing, and regulatory drug submissions.
- Advanced user of SAS software (SAS9-Base) with proven experience in life sciences and clinical trials.
- Familiar in working with CDISC data formats. Experience with the R software platform is a plus.
- General knowledge of clinical drug development and demonstrated knowledge of pharmacokinetics and pharmacology.
- Accuracy and sense of urgency and quality, timely delivery.
- Ability to work on multiple collaborative projects, team player mentality.
- Excellent verbal and written communications skills in English.
- Eager to learn and develop.
Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service, or other characteristic protected by law.
#J-18808-Ljbffr
Associate Scientist, SAS Programmer employer: Certara
Contact Detail:
Certara Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Scientist, SAS Programmer
✨Tip Number 1
Familiarise yourself with CDISC standards, particularly ADaM and SDTM datasets. Understanding these formats will not only help you in the role but also demonstrate your commitment to the field during interviews.
✨Tip Number 2
Brush up on your SAS programming skills, especially SAS9-Base. Consider working on sample projects or contributing to open-source initiatives to showcase your proficiency and practical experience.
✨Tip Number 3
Network with professionals in the biopharmaceutical industry, particularly those involved in data management and clinical trials. Attend relevant webinars or conferences to make connections that could lead to referrals.
✨Tip Number 4
Stay updated on the latest trends in pharmacokinetics and pharmacology. This knowledge will not only enhance your understanding of the role but also impress potential employers during discussions about the industry.
We think you need these skills to ace Associate Scientist, SAS Programmer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in data management, SAS programming, and any work with CDISC data formats. Emphasise your educational background in Pharmaceutical or Life Sciences, Statistics, or related fields.
Craft a Strong Cover Letter: Write a cover letter that specifically addresses the responsibilities and qualifications mentioned in the job description. Mention your experience with SAS software and any familiarity with R, as well as your ability to work collaboratively on projects.
Showcase Your Skills: In your application, clearly outline your skills in quality control, data analysis, and report writing. Provide examples of past projects where you successfully managed datasets or contributed to regulatory submissions.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. Ensure that your communication skills shine through, as excellent verbal and written communication is crucial for this role.
How to prepare for a job interview at Certara
✨Know Your SAS Inside Out
As an Associate Scientist and SAS Programmer, you need to demonstrate your advanced knowledge of SAS software. Be prepared to discuss specific projects where you've used SAS, particularly in relation to CDISC data formats and clinical trials.
✨Showcase Your Teamwork Skills
Since the role involves working closely with other associates and experts, highlight your experience in collaborative projects. Share examples of how you've contributed to team success and managed multiple tasks effectively.
✨Understand the Drug Development Process
Familiarise yourself with the clinical drug development lifecycle and pharmacokinetics. Being able to discuss these topics will show your understanding of the industry and how your role fits into the bigger picture.
✨Prepare for Client Interaction Scenarios
You'll be interacting directly with clients regarding data transfers and specifications. Prepare for potential questions about how you would handle client queries or issues, demonstrating your communication skills and problem-solving abilities.
