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Full-time
bachelor degree
Comprehensive Benefits Package, Competitive Salaries, Departmental Study/Training Budget, Flexible Working Hours, Remote/Hybrid Working Options, Leadership And Mentoring Opportunities
Posted 1d ago
~40 hrs/week
Responsibilities
Lead clinical programming activities for global studies, including the design, validation, and maintenance of clinical databases and data visualization tools. Collaborate cross-functionally to ensure regulatory compliance and drive departmental process improvements and innovation.
Requirements
Requires a degree in Life Science, Healthcare, Computer Science, or a related field with at least 5 years of experience in drug development or clinical research. Must possess expert knowledge of EDC systems, technical data management, and CDISC standards such as SDTM and CDASH.
Full job description
At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.
We're looking for a Senior Clinical Programmer I who thrives on solving complex challenges and transforming clinical data into high-quality, reliable insights that drive drug development. In this role, you'll play a key part in building and maintaining clinical databases, leading programming activities across global studies, and collaborating with cross-functional teams to deliver data that accelerates better outcomes for patients. Beyond study execution, you'll have the opportunity to influence departmental processes, mentor colleagues, and help shape the future of clinical programming within a collaborative and innovation-driven environment.
About the Role As a Senior Clinical Programmer I, you will lead clinical programming activities that support the successful delivery of global clinical studies, ensuring high-quality data capture, database development, and regulatory compliance throughout the study lifecycle. You'll collaborate cross-functionally to design, build, validate, and maintain clinical databases, develop programming solutions and data visualizations, and champion CDISC standards and programming best practices. In addition to managing project timelines, budgets, and deliverables, you'll drive process improvements, contribute to business development activities, and provide technical leadership and mentorship to junior team members.
Your main responsibilities will include but not limited to:
Lead clinical programming activities across assigned studies, ensuring project timelines, budgets, deliverables, and resource needs 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, 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.
About You
If you are a collaborative and 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:
Life science, healthcare, Computer Science and/or related field degree
Minimum 5 years of experience in drug development and/or clinical research
Good understanding and hands-on experiences of CDISC standards (i.e. CDASH, TAUGs and SDTM models)
Expert with electronic data capture (EDC) software systems and other tools for managing clinical studies
Expert in technical data management practices (developing programs, validation plans, testing, and documentation)
About Allucent
Our mission is to help bring new therapies to light. When you work at Allucent, that means rolling up your sleeves and applying your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life-improving treatments.
If you're passionate about helping customers develop new pharmaceuticals and biologics; have an entrepreneurial spirit; and ready to join other science, business, and operations leaders, we would love to get to learn more about how we can help each other grow.
Together we SHINE. Find more information about our values.
Benefits of working at Allucent include:
Comprehensive benefits package per location
Competitive salaries per location
Departmental Study/Training Budget for furthering professional development
Flexible Working hours (within reason)
Opportunity for remote/hybrid working depending on location
Leadership and mentoring opportunities
Participation in our enriching Buddy Program as a new or existing employee
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 going above and beyond on projects
Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees
Apply now!
If you are interested in this role please apply through the button or for more information reach out to Demetria Eggleston at [email protected]
Disclaimers:
Our policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within a reasonable distance from one of our global offices.
“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”
Allucent is on a mission to help bring new therapies to light by solving the distinct challenges of small and mid-sized biotech companies. The company is purpose-built through the convergence of leading providers to address this unmet need. Today, Allucent is a global provider of comprehensive drug development solutions, including consulting, clinical operations, biometrics and clinical pharmacology across a variety of therapeutic areas. With more than 30 years of experience in over 60 countries, Allucent’s individualized partnership approach provides experience-driven insights and expertise to assist its clients in successfully navigating the complexities of delivering novel treatments to patients.
Offices: 2000 Centregreen Way, Suite 300, Cary, North Carolina 27513, US · Habarzel Street, 2, Tel Aviv, 6971002, IL · Walaardt Sacrestraat 401-403, 1117 BM, Schiphol, NL · Fourways 2055, Johanesburg, ZA · Cara Urosa 26/3, Belgrade, 11000 , RS
Drug DevelopmentRegulatory Affairs and SubmissionsClinical StrategyCell & Gene TherapyRare Diseases & Orphan IndicationsOncology & HematologyStudy startup & FeasibilityRegulatory StrategySmall and midsized biotech companiesBiostatistics
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