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- Tasks: Lead clinical programming activities and ensure high-quality data management for impactful healthcare solutions.
- Company: Join Johnson & Johnson, a leader in healthcare innovation and inclusivity.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Other info: Dynamic work environment with a focus on innovation and career development.
- 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 in High Wycombe employer: J&J Family of Companies
Contact Detail:
J&J Family of Companies 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 folks in the industry, especially those at Johnson & Johnson. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for interviews by brushing up on your technical skills. Make sure you can talk confidently about programming languages and data structures relevant to the role. We want to see your expertise shine!
✨Tip Number 3
Showcase your problem-solving skills! Be ready to discuss how you've tackled complex data challenges in the past. We love hearing about real-life examples that demonstrate your analytical prowess.
✨Tip Number 4
Don't forget to apply through our website! It's the best way to ensure your application gets noticed. Plus, it shows you're genuinely interested in joining our team at Johnson & Johnson.
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 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! Mention your experience with CDISC standards, data model specifications, and any programming languages you’re proficient in. We love seeing candidates who are data-savvy and detail-oriented.
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, we love seeing applications come directly from our site!
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 topics 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
Research Johnson & Johnson's commitment to diversity and inclusion. Be ready to discuss how you can contribute to an inclusive work environment and respect for individual merit. This will help you align your values with theirs during the interview.
✨Ask Insightful Questions
Prepare thoughtful questions about the team dynamics, ongoing projects, and how they implement new technologies in their clinical trials. This not only shows your interest in the role but also gives you a better understanding of what to expect if you join their team.