Clinical Programmer Apply now

Clinical Programmer

Nottingham Full-Time 36000 - 60000 £ / year (est.)
Apply now
W

At a Glance

  • Tasks: Join a dynamic team to oversee clinical programming from study setup to submission-ready packages.
  • Company: Work with a leading global CRO that values performance and innovation.
  • Benefits: Enjoy a fully remote role with generous salary, annual pay rise, and personal development focus.
  • Why this job: Be part of exciting studies in a supportive environment that encourages teamwork and individuality.
  • Qualifications: Bachelor’s degree in relevant fields; strong SAS programming and clinical trial experience required.
  • Other info: Interviews available immediately; apply now to join a dedicated Pharma team!

The predicted salary is between 36000 - 60000 £ per year.

Clinical Programmer – FSP | Global Leading CRO | UK | Home Based | A leading global CRO is hiring a Clinical Programmer to join their team. You’ll be fully integrated into a dedicated sponsor that values performance, recognizes merit, and prioritizes quality. This supportive environment encourages innovation, individuality, and teamwork. The role is fully remote. What you will be doing: Collaborate with Data Managers and Clinical Standards teams to provide expertise, delivery and oversight of clinical programming deliverables from study set-up to submission-ready tabulation packages. Provide specifications for data models to be used for quality review and for final data model (SDTM); design mapping algorithms for non-standard conversions. Ensure datasets meet quality standards (e.g., Pinnacle 21 checks), are ready for stakeholder use (medical review, monitoring, adaptive designs), and compliant for database lock. Program quality review checks and reports for use by Data Managers and other team members. Develop and maintain working knowledge and expertise in programming languages utilized in clinical programming (SAS, SQL). Create submission-ready SDTM packages for FDA or other regulatory authorities. Acquire and maintain working knowledge in data collection tools such as Medidata Rave, LSAF, Pinnacle 21. Work to CDISC standards such as SDTM, CDASH, Controlled Terminology and define.xml. What you will need: Bachelor’s degree or equivalent in computer science, mathematics, statistics, data science/analytics, or other relevant scientific. Technically capable, a strong communicator, highly organized and have strong project management skills. Clinical Programming experience and experience working on a clinical trial. Expert knowledge of SAS Programming, Define.xml, SDTM aCRF, cSDRGs. Expert knowledge of data structures. Right to work in the UK. What you will receive: Work for a world leading CRO for a dedicated Pharma. Focus on employee personal development and training. Work on exciting and innovative studies. Generous salary and annual pay rise. Fully home based in the UK or across Europe. Interviews immediately available. What to do next: If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the Clinical Programmer onboard as soon as possible. Not what you’re looking for? Please contact Jo Fornaciari on +44 7488 822 859 for a confidential discussion about potential opportunities.

Clinical Programmer employer: Warman O'Brien

Join a leading global CRO that champions innovation and teamwork in a fully remote environment. With a strong focus on employee development, competitive salaries, and the opportunity to work on groundbreaking studies, this role as a Clinical Programmer offers a rewarding career path where your contributions are valued and recognized. Experience a supportive culture that prioritizes quality and empowers you to excel in your field.
W

Contact Detail:

Warman O'Brien Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Programmer

✨Tip Number 1

Make sure to highlight your experience with SAS and SQL during the interview. These programming languages are crucial for the role, and demonstrating your expertise can set you apart from other candidates.

✨Tip Number 2

Familiarize yourself with CDISC standards, especially SDTM and Define.xml. Being able to discuss these standards confidently will show that you are well-prepared for the responsibilities of the position.

✨Tip Number 3

Prepare examples of how you've collaborated with Data Managers or Clinical Standards teams in past projects. This will demonstrate your teamwork skills and ability to deliver quality results in a clinical programming context.

✨Tip Number 4

Since the role is fully remote, be ready to discuss your project management skills and how you stay organized while working independently. This will reassure the hiring team of your ability to thrive in a home-based environment.

We think you need these skills to ace Clinical Programmer

SAS Programming
SQL
Data Modeling
SDTM
CDASH
Controlled Terminology
Define.xml
Data Quality Assurance
Clinical Trial Experience
Project Management
Communication Skills
Attention to Detail
Problem-Solving Skills
Knowledge of Data Collection Tools (e.g., Medidata Rave, LSAF, Pinnacle 21)
Collaboration Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your relevant experience in clinical programming, particularly with SAS and SDTM. Emphasize any previous roles where you collaborated with Data Managers or worked on clinical trials.

Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention specific projects or experiences that demonstrate your expertise in programming languages and your ability to meet quality standards.

Showcase Technical Skills: Clearly outline your technical skills related to clinical programming, including your proficiency in SAS, SQL, and familiarity with data collection tools like Medidata Rave. Provide examples of how you've applied these skills in past projects.

Highlight Project Management Abilities: Since strong project management skills are essential for this role, include examples of how you've successfully managed projects in the past. Discuss your organizational skills and ability to work collaboratively in a team environment.

How to prepare for a job interview at Warman O'Brien

✨Showcase Your Technical Skills

Make sure to highlight your expertise in SAS programming, SQL, and your understanding of data structures. Be prepared to discuss specific projects where you utilized these skills, as this will demonstrate your technical capability.

✨Understand CDISC Standards

Familiarize yourself with CDISC standards such as SDTM and CDASH. During the interview, be ready to explain how you've applied these standards in previous roles, as this knowledge is crucial for the position.

✨Communicate Clearly

As a Clinical Programmer, strong communication skills are essential. Practice explaining complex programming concepts in simple terms, as you may need to collaborate with Data Managers and other team members who may not have a technical background.

✨Demonstrate Project Management Skills

Be prepared to discuss your experience in managing clinical programming projects. Highlight your organizational skills and any tools or methodologies you use to keep projects on track, as this will show your ability to handle responsibilities effectively.

W
  • Clinical Programmer

    Nottingham
    Full-Time
    36000 - 60000 £ / year (est.)
    Apply now

    Application deadline: 2026-12-12

  • W

    Warman O'Brien

  • Other open positions at Warman O'Brien

    W
    Senior Statistical Programmer

    Warman O'Brien

    Reading Full-Time
Similar positions in other companies
A
Clinical Programmer

AL Solutions

Full-Time 36000 - 60000 £ / year (est.)
P
Senior Director, Clinical Project Leadership

Planet Pharma

Nottingham Full-Time 72000 - 100000 £ / year (est.)
Europas größte Jobbörse für Gen-Z
discover-jobs-cta
Discover now
>