At a Glance
- Tasks: Design and develop SAS programming codes for clinical trials and statistical output reports.
- Company: Join Everest Clinical Research, a leading global contract research organisation.
- Benefits: Work remotely from anywhere in the UK with competitive salary and growth opportunities.
- Other info: Be part of a supportive team focused on quality and customer service.
- Why this job: Make a real impact in the pharmaceutical industry while working on innovative projects.
- Qualifications: Experience in SAS programming and a passion for clinical research.
Everest Clinical Research is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.
Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan.
To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Statistical Programmer remotely from a home-based office anywhere in the UK in accordance with our Work from Home policy.
- Design and specify study data tabulation models and analysis data models for clinical trials or for the integration of clinical trial data from multiple trials.
- Generate complete and efficient analysis data models following approved dataset designs or specifications.
- Develop SAS programming codes and generate complete and accurate statistical output reports of trial data in well-defined formats.
- Develop SAS programming codes to independently validate statistical output reports of trial data generated by other programmers or statisticians.
- Develop and test SAS codes for clinical trial database logical checks and reports for ongoing data review.
- Document data and programming information in accordance with corporate SOPs and guidelines.
- Archive clinical trial data (study data tabulation models and analysis data models) and programming information in accordance with corporate archival SOPs and guidelines.
- Develop and provide expertise in other programming and system administration areas when required.
- Provide technical guidance and support to less experienced Statistical Programmers.
- Contribute to the continuous improvement of the statistical programming processes and procedures.
- Contribute to the establishment of therapeutic area programming standards/conventions/procedures within assigned therapeutic areas as a lead programmer.
- Contribute to the establishment of client specific programming standards/conventions/procedures for assigned clients when required.
We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.
Senior SAS Programmer (Pharmaceutical) employer: Everest Clinical Research
Everest Clinical Research is an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of biostatistics. With a focus on employee growth, we provide ample opportunities for professional development and advancement, all while working remotely from the picturesque Croxley Green, UK. Join us to be part of a team that values quality, efficiency, and meaningful contributions to clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Senior SAS Programmer (Pharmaceutical)
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Everest Clinical Research. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Everest Clinical Research.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Everest Clinical Research. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
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When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Everest Clinical Research is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Senior SAS Programmer (Pharmaceutical)
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Everest Clinical Research!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Everest Clinical Research that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Everest Clinical Research!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Everest Clinical Research, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Everest Clinical Research
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Everest Clinical Research that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Everest Clinical Research’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
