Experienced Clinical Programmer in High Wycombe

Experienced Clinical Programmer in High Wycombe

High Wycombe Full-Time 46000 - 52000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Lead clinical programming activities and develop innovative data solutions for healthcare.
  • Company: Join Johnson & Johnson, a leader in healthcare innovation and inclusivity.
  • Benefits: Competitive salary, inclusive environment, and opportunities for professional growth.
  • Other info: Dynamic role with opportunities to improve processes and drive innovation.
  • Why this job: Make a real impact on health by working with cutting-edge technologies in clinical trials.
  • Qualifications: Experience in clinical programming, data management, and strong analytical skills.

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. 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 creates and executes edit check programs, listings and report solutions to aid in monitoring of safety, risk, compliance and ensures quality data review.

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 Clinical Programmer in High Wycombe employer: Johnson & Johnson

At Johnson & Johnson, we foster a culture of innovation and inclusivity, making it an exceptional employer for those in the healthcare sector. Our commitment to employee growth is evident through continuous learning opportunities and a supportive environment that values diversity and individual contributions. Located in High Wycombe, Buckinghamshire, our team enjoys a collaborative atmosphere where cutting-edge healthcare solutions are developed, ensuring that every employee plays a vital role in improving health outcomes globally.

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Contact Details:

Johnson & Johnson Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Experienced Clinical Programmer in High Wycombe

Tip Number 1

Network like a pro! Reach out to your connections in the healthcare and programming fields. Attend industry events or webinars, and don’t be shy about asking for introductions. We all know someone who knows someone, and that could be your ticket in!

Tip Number 2

Prepare for those interviews by brushing up on your technical skills and understanding the latest trends in clinical programming. We recommend practising common interview questions and even doing mock interviews with friends. Confidence is key!

Tip Number 3

Showcase your projects! If you’ve worked on any relevant clinical trials or programming tasks, make sure to highlight them in your discussions. We want to see how your experience aligns with what Johnson & Johnson is looking for.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in being part of the Johnson & Johnson team. Let’s get you that job!

We think you need these skills to ace Experienced Clinical Programmer in High Wycombe

Clinical Trial Programming
Data Management
CDISC SDTM
Data Modeling
Programming Languages
Edit Check Programs
Report Writing

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 any relevant data management skills. We want to see how your background aligns with our needs!

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 skills can contribute to our mission at Johnson & Johnson. Keep it engaging and personal – we love a good story!

Showcase Your Technical Skills:Don’t forget to highlight your technical capabilities in programming and data management. Mention specific tools or languages you’re proficient in, especially those related to CDISC standards and clinical data reporting. We’re looking for someone who can hit the ground running!

Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the details you need about the role and our company culture there!

How to prepare for a job interview at Johnson & Johnson

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. Prepare examples of how you've tackled complex data structures in past projects.

Understand CDISC Standards

Familiarise yourself with CDISC submission standards, particularly SDTM tabulation packages. You might be asked about your experience in creating or reviewing these packages, so having specific examples ready will show that you know your stuff and can hit the ground running.

Showcase Your Problem-Solving Skills

Prepare to discuss how you've identified gaps in project requirements and proposed solutions in previous roles. Think of a couple of scenarios where your analytical reasoning made a significant impact on a project’s success, as this aligns well with the responsibilities of the role.

Emphasise Team Collaboration

Since the role involves oversight and collaboration, be ready to talk about your experience working in teams. Highlight any leadership roles you've taken on and how you’ve contributed to improving processes or tools within your team. This will demonstrate your ability to work well in an inclusive environment.