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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 collaborative 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 data programming is essential.
- 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 can set you apart from other candidates.
✨Tip Number 2
Highlight any experience you have with clinical data structures and how you've presented data for clinical review in past roles. This will show that you understand the nuances of the role and can hit the ground running.
✨Tip Number 3
Prepare to discuss your experience with process improvement initiatives. Be ready to share specific examples of how you've contributed to enhancing workflows or SOPs in previous positions.
✨Tip Number 4
Since this role involves mentoring junior team members, think about your coaching experiences. Be prepared to talk about how you've supported others in their development and how you can bring that to our team.
We think you need these skills to ace Senior Statistical Programmer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical data programming, particularly within the pharmaceutical industry or clinical research organizations. Emphasize your skills with SAS Macros and any experience with CDISC SDTM.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical programming and your ability to manage timelines and quality. Mention specific examples of how you've contributed to process improvements or mentored junior team members.
Highlight Communication Skills: Since the role involves participating in sponsor meetings and presenting processes, ensure you demonstrate your excellent verbal and written communication skills in your application materials.
Showcase Problem-Solving Abilities: Include examples in your application that illustrate your ability to provide technical solutions to data issues during study conduct and analysis. This will show your proactive approach to potential challenges.
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.
