Allucent
Senior Clinical Programmer I
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Senior Clinical Programmer I – Drug Development Specialisation
At Allucent™, we empower small to medium biopharmaceutical companies to tackle the intricacies of clinical trials, accelerating the development of life-changing therapies for global patients.
We’re seeking a Senior Clinical Programmer I – a strategic problem-solver who ingeniously transforms clinical data into high-value insights. This role is pivotal in designing and refining clinical databases, guiding programming projects across international studies, and collaborating with cross-functional teams to ensure premium data integrity. Beyond execution, you’ll shape departmental processes, mentor your peers, and foster innovation in this dynamic, data-led environment.
About the Role
As a Senior Clinical Programmer I, you’ll lead clinical programming initiatives from conceptualisation to closeout, critical for the successful execution of global clinical trials. Your responsibilities will encompass:
- Clinical Database Authoring & Compliance: Develop, validate, and maintain high-integrity clinical databases, incorporating electronic data checks, clinical data listings, and visual analytics tools – all while ensuring efficacy and regulatory alignment with CDISC standards.
- Cross-functional Collaboration: Work seamlessly with Data Management, Project Management, Biostatistics, and broader clinical teams to design documentation, refine technical specifications, and deliver programming solutions that enhance efficiency and minimise risk.
- Standards & Quality Champion: Mobile interns with the CDISC ecosystem (CDASH, SDTM, and ADaM)—penciling best practices for consistent programming, query management, and inspection-ready data edits.
- Process & Innovation Driver: Advocate continuous improvement by identifying bottlenecks, shaping global programming frameworks, automating workflows, and integrating next-gen data analytics to advance clinical research.
You’ll own programmatic budgets, timelines, deliverable quality, and stakeholder relations, while also acting as a technical mentor to junior team members, fostering growth in a collaborative, innovation-driven culture.
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Main Responsibilities
Your work will span critical phases of clinical trials, including:
-
Project Ownership:
- Oversee clinical programming activities for assigned studies, managing risks, changes, and resources.
- Escalate challenges proactively to stakeholders and guide resolution.
-
Database Development & Validation:
- Build, test, and refine electronic data capture (EDC)-aligned, CDISC-/SDTM-compliant databases.
- Develop intricate programming tools, such as special character functions (SCF), data listings, and data visualisation for analysis.
-
Study Cycle Standardization:
- Ensure consistency in database designs, validation processes, and edit rules across global studies.
- Conform to regulatory guidelines and operational best practices including SDTM and CDASH templates, use of mgmt datasets.
-
Innovation & Process Optimization:
- Propose enhancements to workflows, efficiency, and data integrity intuitively.
- Drive adoption of data visualisation tools and integrate validation platforms to streamline delivery phases.
-
Knowledge Sharing:
- Lead cross-departmental work groups to improve clinical data programming standards.
- Train and mentor junior programmers, sharing knowledge on CDISC, query management, and validation techniques.
About You
We’re seeking a hands-on clinical programmer who specialises in:
- Life Sciences or Computer Science graduate with extensive clinical trial knowledge.
- Minimum 5 years of experience in pharmaceutical drug development or clinical research—spearheading end-to-end programming initiatives.
- Strong CDISC proficiency, with practical exposure to CDASH (v10/11), SDTM models (SDTMIG Version 5/6), and compliance with shadow datasets.
- EDC expertise, including software handling at scale (e.g., OpenClinica, Vistra, or other platforms).
- Technical aptitude: Adept at reshaping data structures, implementing tests (automated/repetitive), and generating adaptable, future-proof documentation.
Bonus: passion for patient-centred innovation and experience in integrating data analytics or advanced datalakes into clinical research.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
At Allucent
Our partnership with clients begins with a shared pursuit of medical advancement. Staff turn out applied expertise, customising end-to-end solutions tailored to biopharma’s evolving needs—turning obstacles into leadership.
Core Values:
- Self-determination: Own your ambitions and push forward.
- Limestone-driven: Integrity breeds excellence.
- Inclusion: Unleash our workforce’s full potential.
Allucent operates not as a silo, but as a thriving community where science and business blend at evolving crossroads.
Benefits
An Allucent career rewards innovation and excellence with:
✔ Holistic benefits (per location) that prioritise health and balance. ✔ Competitive salary, equally dependent on demand and focus area. ✔ Department wide Training/Study Budget: Grow skills with continuous learning initiatives. ✔ Flexible schedules (with in-office commitment set at 2/5 days post-authorisation). ✔ Options for hybrid and remote work models (depends on job location). ✔ Leadership and mentorship opportunities for nurturing high-performers. ✔ Buddy programme: Foster camaraderie and fresh perspectives. ✔ Growth & progression: Clear upward trajectory within Allucent. ✔ Spot & Loyalty Bonus Programmes for going the extra mile. ✔ Access to advanced soft-skills/technical training through internal platforms. ✔ Profit-sharing referral bonuses for whole-team performance.
Let’s SHINE together.
Work at Allucent™ and make an enduring impact in pharmaceutical research.
To apply: Click to apply [link] or reach out directly to Demetria Eggleston, Social Recruiter at Demetria.Eggleston@allucent.com.
For the most current updates, explore their Career Portal.
Employee Note: Policies & Processes: Alluncen disasters does not consider or discuss any unofficial recruitment bids forwarded from third parties. Always submit candidates through official channels. Uncoordinated applications may risk non-remuneration and delayed communication.
#LI-DH-1 #LI-Remote #LI-Hybrid
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills