At a Glance
- Tasks: Lead clinical programming activities and ensure high-quality data management for impactful healthcare solutions.
- Company: Join Johnson & Johnson, a leader in healthcare innovation with a commitment to diversity.
- Benefits: Inclusive work environment, competitive salary, and opportunities for professional growth.
- Other info: Dynamic role with opportunities to innovate and improve healthcare outcomes.
- Why this job: Make a real difference in healthcare by working on cutting-edge clinical trials.
- Qualifications: Experience in clinical programming and strong analytical skills required.
The predicted salary is between 46000 - 52000 € per year.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function: Data Analytics & Computational Sciences
Job Sub Function: Biostatistics
Job Category: Scientific/Technology
All Job Posting Locations: High Wycombe, Buckinghamshire, United Kingdom
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 or 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.
Required Skills:
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 employer: J&J Family of Companies
At Johnson & Johnson, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work environment in High Wycombe, Buckinghamshire. Our commitment to employee growth is reflected in our robust training programmes and opportunities for advancement within the healthcare innovation sector. Join us to be part of a team that values diversity, fosters collaboration, and is dedicated to making a profound impact on health for humanity.
Contact Detail:
J&J Family of Companies Recruiting Team
StudySmarter Expert Advice🤫
We think this is how you could land Experienced Clin Programmer
✨Tip Number 1
Network like a pro! Reach out to folks in your field on LinkedIn or at industry events. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by practising common questions and showcasing your skills. We recommend using the STAR method to structure your answers – it’s a game changer!
✨Tip Number 3
Don’t just apply and wait! Follow up on your applications after a week or so. A quick email can show your enthusiasm and keep you on their radar.
✨Tip Number 4
Check out our website for job openings and apply directly there. It’s the best way to ensure your application gets noticed by the right people!
We think you need these skills to ace Experienced Clin Programmer
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 trial programming, data structures, and any relevant programming languages. We want to see how your skills align with what we’re looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about healthcare innovation and how your background makes you a great fit for our team. Let us know what excites you about the role and Johnson & Johnson!
Showcase Your Technical Skills:Don’t forget to highlight your technical capabilities in your application. Mention specific programming languages, data management tools, and any experience with CDISC standards. We love seeing candidates who are data-savvy and detail-oriented!
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and ensure it gets into the right hands. Plus, you’ll find all the info you need about the role there!
How to prepare for a job interview at J&J Family of Companies
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical programming and data management. Familiarise yourself with industry standards like CDISC and SDTM, as well as the specific programming languages mentioned in the job description. Being able to discuss these confidently will show that you're serious about the role.
✨Showcase Your Problem-Solving Skills
Prepare examples from your past experiences where you've identified gaps in processes or proposed solutions that improved efficiency. Johnson & Johnson values innovation, so demonstrating your analytical reasoning and ability to enhance programming tasks will set you apart.
✨Understand the Company Culture
Johnson & Johnson prides itself on inclusivity and respect for diversity. Research their Credo and be ready to discuss how your values align with theirs. This will help you connect on a personal level during the interview and show that you’re a good fit for their team.
✨Prepare Questions
Have a few thoughtful questions ready to ask at the end of your interview. Inquire about their current projects in innovative medicine or how they ensure compliance with changing regulatory requirements. This shows your genuine interest in the role and the company’s mission.
