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About the role
- Senior Clinical Programmer I leading programming activities contributing to successful global clinical studies at Allucent. Ensuring high-quality data and regulatory compliance throughout the study lifecycle.
Responsibilities
- **About the Role**
- As a **Senior Clinical Programmer I**, you will lead clinical programming activities that contribute to the successful delivery of global clinical studies, ensuring high-quality data capture, database development, and regulatory compliance throughout the study lifecycle. You will collaborate cross-functionally to design, build, validate, and maintain clinical databases, develop programming solutions and data visualizations, and promote CDISC standards and programming best practices. In addition to managing project timelines, budgets, and deliverables, you will drive process improvements, support business development activities, and provide technical leadership and mentorship to junior team members.
- **Your main responsibilities will include but are not limited to:**
- Lead clinical programming activities across assigned studies, ensuring project timelines, budgets, deliverables, and resource requirements are effectively managed while proactively identifying and escalating risks or change orders.
- Design, build, validate, and maintain clinical databases, electronic edit checks, data listings, and data visualization tools to support high-quality data collection, review, and regulatory compliance.
- Collaborate cross-functionally with Data Management, Project Management, Biostatistics, and study teams to develop study documentation, clarify technical specifications, and deliver programming solutions that meet project objectives.
- Champion industry standards and quality by applying CDISC conventions (CDASH, SDTM, TAUGs), validation principles, and programming best practices to ensure consistent, compliant, and inspection-ready deliverables.
- Drive innovation and continuous improvement by leading process enhancements, developing global programming standards and libraries, implementing data analytics and visualization tools, and supporting departmental initiatives.
Requirements
- **About You**
- If you are a collaborative, detail-oriented clinical programming professional who enjoys solving complex technical challenges and takes pride in delivering high-quality, compliant data solutions that support global clinical trials, this role will give you the opportunity to combine strong expertise in clinical database programming, CDISC standards, and cross-functional collaboration with a passion for continuous improvement, mentoring others, and driving innovation in clinical data management.
- **To be successful we are looking for the following traits and behaviors:**
- Degree in life sciences, healthcare, Computer Science, or a related field
- Minimum 5 years of experience in drug development and/or clinical research
- Good understanding of and hands-on experience with CDISC standards (e.g., CDASH, TAUGs, and SDTM models)
- Expertise with electronic data capture (EDC) systems and other clinical study management tools
- Proficiency in technical data management practices (developing programs, validation plans, testing, and documentation)
Benefits
- **Benefits of working at Allucent include:**
- Comprehensive benefits package per location
- Competitive salaries per location
- Departmental study/training budget to support professional development
- Flexible working hours (within reason)
- Opportunity for remote/hybrid working depending on location
- Leadership and mentoring opportunities
- Participation in our Buddy Program for new and existing employees
- Internal growth opportunities and career progression
- Financially rewarding internal employee referral program
- Access to online soft-skills and technical training via internal platforms
- Eligibility for our Spot Bonus Award Program in recognition of exceptional project contributions
- Eligibility for our Loyalty Award Program in recognition of long-term commitment and service
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