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- Tasks: Lead clinical data transformations and ensure high-quality delivery of reports and visualizations.
- Company: Join a top-tier clinical research organization focused on advancing medicine.
- Benefits: Enjoy remote work flexibility and a supportive team environment.
- Why this job: Make a real impact in healthcare while mentoring others and improving processes.
- Qualifications: A-levels or equivalent; experience in clinical programming and strong SAS skills required.
- Other info: Opportunity to engage with sponsors and participate in audits.
The predicted salary is between 36000 - 60000 £ per year.
Senior Clinical Programmer – Home-Based, UK
We are seeking an experienced Senior Clinical Programmer to join a dynamic Biometrics team within a leading clinical research organization.
This is a permanent, full-time role that offers the flexibility of working remotely within the UK.
About the Role
As a Senior Clinical Programmer, you will play a crucial role in ensuring the timely and high-quality delivery of clinical data transformations, reports, and visualizations.
You will work with multiple data sources to support ongoing data review for both internal teams and external stakeholders.
This position requires a team-oriented professional with strong time management skills and the ability to build effective relationships with sponsors and colleagues.
You will have the opportunity to contribute to process improvements, mentor junior team members, and engage with sponsors through meetings and audits.
Key Responsibilities
- Oversee and manage timelines and quality for assigned studies, proactively addressing potential issues.
- Participate in sponsor meetings, project kick-offs, and audits, presenting clinical programming processes as required.
- Support process improvement initiatives and contribute to the review and update of standard operating procedures (SOPs).
- Act as the primary point of contact for clinical programming tasks and issues on allocated studies.
- Develop specification documents and related study documentation.
- Create and manage data transfer plans for third-party data sources.
- Extract and manipulate clinical trial data using relevant programming languages and tools.
- Develop and validate reports, visualizations, and listings to support clinical data management and review.
- Ensure smooth integration and validation of electronic third-party data.
- Provide technical solutions to data issues that arise during study conduct and analysis.
Required Skills & Experience
Essential:
- Minimum A-levels (or equivalent qualification).
- Prior experience in clinical data programming within the pharmaceutical industry or a clinical research organization.
- Strong understanding of clinical data structures and how to present data for clinical review.
- Experience with SAS Macros and/or other scripting languages.
- Ability to debug SAS programs or similar scripting tools.
- Excellent verbal and written communication skills.
- Strong organizational and time management skills with exceptional attention to detail.
Desirable:
- Degree in a science or mathematics-related field.
- Experience with CDISC Study Data Tabulation Model (SDTM).
- Previous work in oncology or rare disease clinical trials.
- Coaching and mentoring experience.
- Familiarity with clinical trial budgets and tracking out-of-scope activities.
- Participation in sponsor meetings, kick-off meetings, and audits.
- Experience in process improvement initiatives.
Why Join Us?
This is a fantastic opportunity to work in a collaborative and innovative environment that is dedicated to advancing medicine and improving patients’ lives.
If you are passionate about clinical programming and eager to make an impact, we encourage you to apply.
To express interest in this role, please submit your application today!
Senior Statistical Programmer employer: Meet Life Sciences
Contact Detail:
Meet Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Statistical Programmer
✨Tip Number 1
Familiarize yourself with the specific programming languages and tools mentioned in the job description, especially SAS Macros. Being able to demonstrate your proficiency in these areas during interviews will set you apart from other candidates.
✨Tip Number 2
Highlight any experience you have with clinical data structures and the CDISC SDTM model. Be prepared to discuss how you've applied this knowledge in previous roles, as it shows your understanding of the clinical programming landscape.
✨Tip Number 3
Since this role involves mentoring junior team members, think about examples from your past where you've successfully coached or guided others. Sharing these experiences can demonstrate your leadership skills and team-oriented mindset.
✨Tip Number 4
Prepare for potential sponsor meetings by practicing how to present clinical programming processes clearly and effectively. This will not only boost your confidence but also show that you're ready to engage with stakeholders right from the start.
We think you need these skills to ace Senior Statistical Programmer
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Senior Clinical Programmer position. Make sure you understand the key responsibilities and required skills, as this will help you tailor your application effectively.
Highlight Relevant Experience: In your CV and cover letter, emphasize your prior experience in clinical data programming, particularly within the pharmaceutical industry or a clinical research organization. Mention specific projects or tasks that align with the responsibilities outlined in the job description.
Showcase Technical Skills: Clearly outline your proficiency with SAS Macros and any other relevant programming languages or tools. Provide examples of how you've used these skills to solve problems or improve processes in previous roles.
Communicate Effectively: Since excellent verbal and written communication skills are essential for this role, ensure that your application is well-written and free of errors. Use clear and concise language to convey your qualifications and enthusiasm for the position.
How to prepare for a job interview at Meet Life Sciences
✨Showcase Your Technical Skills
Be prepared to discuss your experience with SAS Macros and other scripting languages. Highlight specific projects where you successfully extracted and manipulated clinical trial data, as this will demonstrate your technical proficiency.
✨Emphasize Team Collaboration
Since the role requires strong teamwork, share examples of how you've effectively collaborated with colleagues and sponsors in previous roles. Discuss any experiences where you mentored junior team members or contributed to process improvements.
✨Prepare for Sponsor Meetings
Familiarize yourself with the types of discussions that occur during sponsor meetings and audits. Be ready to present your understanding of clinical programming processes and how you can contribute to successful project outcomes.
✨Demonstrate Attention to Detail
Given the importance of quality in clinical data delivery, prepare to discuss how you ensure accuracy in your work. Provide examples of how your organizational skills have helped you manage timelines and address potential issues proactively.
