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For Companies At a Glance
- Tasks: Lead clinical programming activities and ensure quality data management for impactful clinical trials.
- Company: Join a leading organisation in biostatistics and data analytics.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Make a difference in healthcare by ensuring data integrity in clinical trials.
- Qualifications: Experience in clinical programming and strong analytical skills required.
- Other info: Dynamic work environment with a focus on innovation and compliance.
The predicted salary is between 36000 - 60000 £ per year.
Position Summary
The Experienced Clinical Programmer is an experienced clinical trial programmer with in-depth knowledge in industry standard and complex data structures, programming languages, and/or reporting solutions with proven technical capabilities in leading clinical trial activities and/or teams in accordance with departmental processes and procedures. The position is responsible for oversight of the development of one or more clinical data management trial activities of moderate to high complexity/criticality, including data model specifications, data stream integrations and transformation of source to internal data models and/or CDISC submission ready SDTM tabulation packages (aCRF, define.xml, cSDRG, etc). Creates and executes edit check programs, listings and report solutions to aid in monitoring of safety, risk, compliance and ensures quality data review. Performs reporting solutions role creating study-specific reports translating clinical study team needs into specifications aggregating clinical data sources into custom data and report to monitor safety, risk and compliance.
Role And Responsibilities
- Accountable for one or more clinical programming trial activities of moderate to high complexity, scope and/or criticality.
- Performs comprehensive review of, and provides input into, project requirements and documentation.
- Identifies gaps, proposes solutions and applies expertise to improve efficiency of programming tasks and/or improve overall quality of programming deliverables.
- Ensures latest standards are being utilized, current technologies are deployed.
- Create and/or review specifications for mapping internal data review model for fit for purpose reporting and/or as well as submission ready CDISC SDTM.
- Design mapping algorithms for nonstandard conversions.
- Responsible for creation or review of internal data model for fit for purpose reporting consumption and/or submission ready CDISC SDTM packages for health authority submissions and keeping abreast in changing regulatory requirements.
- Program, or oversight of quality review checks, study specific reports for use by team members and consumers of data.
- May perform role that programmatically aggregates clinical data sources into custom data model for fit for purpose consumption study specific report solutions performing appropriate quality control and verification in support of assigned reporting activities.
- Support and/or lead in developing and implementing process, system and tool improvement initiatives within compliance with departmental processes and procedures.
Preferred Skills
- Advanced Analytics
- Analytical Reasoning
- Biological Sciences
- Biostatistics
- Clinical Trials
- Data Modeling
- Data Privacy Standards
- Data Quality
- Data Savvy
- Detail-Oriented
- Good Clinical Practice (GCP)
- Report Writing
- Research Ethics
- Researching
- Statistical Analysis Systems (SAS) Programming
- Statistics
- Technologically Savvy
Experienced Clin Programmer in High Wycombe employer: Johnson & Johnson Innovative Medicine
Contact Detail:
Johnson & Johnson Innovative Medicine Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Experienced Clin Programmer in High Wycombe
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical programming field. Attend industry events or webinars, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for interviews by brushing up on your technical skills. Make sure you can talk confidently about data structures, programming languages, and reporting solutions. We recommend practising common interview questions related to clinical trials and data management.
✨Tip Number 3
Showcase your projects! If you’ve worked on any clinical trial activities or developed reporting solutions, make sure to highlight these in your discussions. We love seeing real examples of your work and how you’ve contributed to improving efficiency and quality.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for talented individuals who are passionate about biostatistics and data analytics. Let’s get you on board!
We think you need these skills to ace Experienced Clin Programmer in High Wycombe
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Experienced Clinical Programmer role. Highlight your experience with clinical trials, programming languages, and data management. We want to see how your skills match what we're looking for!
Showcase Your Technical Skills: Don’t hold back on showcasing your technical capabilities! Include specific examples of your work with data models, reporting solutions, and any programming languages you’re proficient in. This is your chance to shine!
Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this role. Share your passion for biostatistics and data analytics, and explain how your previous experiences have prepared you for this position. Keep it engaging!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Johnson & Johnson Innovative Medicine
✨Know Your Programming Languages
Make sure you brush up on the programming languages mentioned in the job description, especially SAS. Be ready to discuss your experience with these languages and how you've used them in clinical trials.
✨Understand Data Structures
Familiarise yourself with industry-standard data structures and CDISC standards. Prepare to explain how you've worked with complex data models and how you ensure data quality and compliance in your previous roles.
✨Showcase Problem-Solving Skills
Be prepared to discuss specific examples where you've identified gaps in project requirements and proposed solutions. Highlight your analytical reasoning and how it has improved programming efficiency or quality in past projects.
✨Stay Updated on Regulatory Changes
Demonstrate your knowledge of current regulatory requirements and how they impact clinical programming. Discuss any recent changes you've adapted to and how you keep abreast of industry developments.