At a Glance
- Tasks: Lead clinical programming activities and ensure quality data management for impactful trials.
- Company: Dynamic biotech firm focused on innovative clinical solutions.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Join a collaborative team dedicated to advancing clinical research.
- Why this job: Make a difference in healthcare by transforming data into actionable insights.
- Qualifications: Experience in clinical programming and strong analytical skills required.
The predicted salary is between 45000 - 55000 £ per year.
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. This includes 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). The role involves creating and executing edit check programs, listings, and report solutions to aid in monitoring safety, risk, compliance, and ensuring quality data review. It also entails performing reporting solutions by creating study-specific reports that translate clinical study team needs into specifications, aggregating clinical data sources into custom data and reports to monitor safety, risk, and compliance.
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 and 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 while keeping abreast of changing regulatory requirements.
- Program, or oversee quality review checks, study specific reports for use by team members and consumers of data.
- May perform a 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.
Required 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
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: 7360-Janssen-Cilag Limited Legal Entity
Join a leading organisation in High Wycombe, where we prioritise innovation and excellence in clinical programming. Our collaborative work culture fosters professional growth, offering extensive training and development opportunities to enhance your skills in data analytics and biostatistics. With a commitment to quality and compliance, we provide a supportive environment that values your contributions and encourages you to make a meaningful impact in the field of clinical trials.
Contact Details:
7360-Janssen-Cilag Limited Legal Entity Recruitment 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 industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to clinical programming. We recommend doing mock interviews with friends or using online resources to get comfortable discussing your experience and skills. The more prepared you are, the more confident you'll feel!
✨Tip Number 3
Showcase your skills through projects or case studies. If you’ve worked on any interesting clinical trials or data management tasks, create a portfolio to demonstrate your expertise. We love seeing real-world applications of your knowledge!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we often have exclusive opportunities listed there that you won’t find anywhere else. So, get clicking!
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 Clin Programmer role. Highlight your experience with clinical trials, data management, and any programming languages you know. We want to see how your skills match what we're looking for!
Showcase Your Projects:Include specific examples of projects you've worked on that relate to the job description. Whether it's creating SDTM packages or developing reporting solutions, we love to see real-world applications of your skills.
Be Clear and Concise:When writing your application, keep it clear and to the point. Use bullet points where possible to make it easy for us to read through your qualifications and experiences. We appreciate a well-structured application!
Apply Through Our Website:Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at 7360-Janssen-Cilag Limited Legal Entity
✨Know Your Data Inside Out
Make sure you have a solid understanding of data structures and programming languages relevant to clinical trials. Brush up on your knowledge of CDISC standards and be ready to discuss how you've applied these in past projects.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've identified gaps in project requirements and proposed effective solutions. Highlight your ability to improve efficiency and quality in programming tasks, as this will demonstrate your analytical reasoning.
✨Be Ready for Technical Questions
Expect questions that dive deep into your technical capabilities, especially around SAS programming and data modelling. Practise explaining complex concepts in simple terms, as this shows your depth of understanding and communication skills.
✨Demonstrate Your Attention to Detail
Clinical programming requires a keen eye for detail. Be prepared to discuss how you ensure data quality and compliance with Good Clinical Practice (GCP). Share specific instances where your attention to detail made a significant impact on a project.
