At a Glance
- Tasks: Prepare and analyse clinical trial data while ensuring quality and compliance.
- Company: Leading clinical research organisation focused on oncology.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real difference in clinical research and patient outcomes.
- Qualifications: Strong SAS and R programming skills with clinical data analysis experience.
- Other info: Collaborative environment with a focus on data quality and innovation.
The predicted salary is between 42000 - 84000 Β£ per year.
A leading clinical research organization is seeking a Senior SAS Programmer with R skills to contribute to clinical trials, especially in oncology. The role involves data preparation, quality control, and collaboration with cross-functional teams to ensure regulatory compliance and address stakeholders' needs.
The ideal candidate will have:
- a strong background in clinical data analysis,
- experience with CDISC standards,
- a commitment to data quality.
This position offers a remote work opportunity and a chance to impact clinical research positively.
Remote Senior SAS & R Programmer for Clinical Trials employer: Coronado Research
Contact Detail:
Coronado Research Recruiting Team
StudySmarter Expert Advice π€«
We think this is how you could land Remote Senior SAS & R Programmer for Clinical Trials
β¨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those who work with SAS and R. Join relevant online forums or LinkedIn groups to connect with others and learn about hidden job opportunities.
β¨Tip Number 2
Show off your skills! Create a portfolio showcasing your previous projects related to clinical trials, data analysis, and any work with CDISC standards. This will give potential employers a clear view of what you can bring to the table.
β¨Tip Number 3
Prepare for interviews by brushing up on common questions related to SAS programming and clinical data analysis. We recommend practising your responses with a friend or using mock interview platforms to build confidence.
β¨Tip Number 4
Donβt forget to apply through our website! We have a range of exciting opportunities that match your skills. Plus, applying directly can sometimes give you an edge over other candidates.
We think you need these skills to ace Remote Senior SAS & R Programmer for Clinical Trials
Some tips for your application π«‘
Tailor Your CV: Make sure your CV highlights your experience with SAS and R, especially in the context of clinical trials. We want to see how your skills align with the job description, so donβt be shy about showcasing your relevant projects!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why youβre passionate about clinical research and how your background fits the role. We love seeing candidates who can connect their experiences to our mission.
Showcase Your Data Quality Commitment: Since data quality is key in this role, make sure to mention any specific methodologies or standards youβve used in past projects. We appreciate candidates who understand the importance of regulatory compliance and CDISC standards.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. Itβs super easy, and weβll be able to review your application more efficiently. Letβs get started on this journey together!
How to prepare for a job interview at Coronado Research
β¨Know Your SAS and R Inside Out
Make sure you brush up on your SAS and R programming skills before the interview. Be prepared to discuss specific projects where you've used these tools, especially in clinical trials. Highlight any experience you have with data preparation and quality control, as this will show your technical expertise.
β¨Familiarise Yourself with CDISC Standards
Since the role requires knowledge of CDISC standards, take some time to review these guidelines. Be ready to explain how you've applied them in past projects. This will demonstrate your commitment to regulatory compliance and your understanding of industry best practices.
β¨Showcase Your Collaborative Spirit
Collaboration is key in this role, so think of examples where you've worked with cross-functional teams. Prepare to discuss how youβve effectively communicated with stakeholders to address their needs. This will highlight your ability to work well in a team-oriented environment.
β¨Emphasise Your Commitment to Data Quality
Data quality is crucial in clinical research, so be ready to talk about your approach to ensuring accuracy and reliability in your work. Share specific instances where you identified and resolved data issues, showcasing your attention to detail and dedication to high standards.