EDC Developer / Programmer – Clinical Data Sciences
💰 $80,000 – $130,000/yr
Job Description
About This Opportunity
Celerion is seeking a skilled, performance-oriented Electronic Data Capture (EDC) Database Developer / Clinical Programmer to join our Clinical Data Sciences team. This is a full-time remote position based in the US, with occasional travel required for training and key meetings. You'll play a critical role in accelerating life-saving drug development through expert EDC system administration and clinical trial support.
About Celerion
Celerion is committed to delivering swift, exceptional clinical research through translational medicine. Our team combines deep experience, operational agility, and innovative research strategies to help pharmaceutical and biotech companies get treatments to market faster. Every project we undertake supports the mission of creating life-saving therapies for patients in need.
Key Responsibilities
- EDC Database Administration: Manage and administer Electronic Data Capture systems for clinical trial projects, ensuring optimal performance and regulatory compliance.
- Protocol & Requirements Evaluation: Analyze study protocols and client requirements to develop comprehensive EDC solutions tailored to project needs.
- Electronic Case Report Form (eCRF) Design & Build: Design, develop, and implement electronic case report forms with corresponding validation edits, ensuring data integrity and usability.
- Vendor & Technical Management: Serve as the primary technical liaison with EDC vendors and supporting applications, troubleshooting issues and escalating problems to appropriate partners.
- Expert Guidance: Provide specialist recommendations and guidance throughout the complete lifecycle—design, development, validation, implementation, and maintenance of study set-up.
- System Deployment: Manage the deployment of EDC trials to production environments, coordinate with cross-functional teams, and establish interface connections between EDC systems and other enterprise applications.
- Analysis & Recommendations: Conduct thorough evaluation and analysis to identify opportunities for improvement and provide actionable recommendations for achieving project goals.
About You
You are a self-motivated team player with a track record of success in fast-paced, dynamic environments. You bring technical expertise in Electronic Data Capture systems, strong problem-solving skills, and a commitment to excellence. You thrive in collaborative settings, communicate effectively with both technical and non-technical stakeholders, and demonstrate initiative in supporting clinical research that matters.
Required Skills & Experience
- Proven experience with Electronic Data Capture (EDC) systems administration and development
- Strong knowledge of eCRF design and clinical trial database principles
- Experience with clinical data management and regulatory compliance standards (21 CFR Part 11, CDISC)
- Technical proficiency in database management and validation processes
- Excellent vendor management and cross-functional communication skills
- Familiarity with system integration and interface development
- Strong analytical and problem-solving abilities in a clinical research context
Why Join Celerion?
Work with a mission-driven organization dedicated to accelerating clinical research and bringing innovative treatments to patients. This role offers the opportunity to apply your technical expertise in a meaningful healthcare context, collaborate with talented clinical research professionals, and contribute directly to life-saving drug development. The remote structure provides flexibility while maintaining strong team connections through in-person meetings and training opportunities.
Work Arrangement
Location: Remote, US-based
Travel: Occasional travel required for training sessions and key meetings
Employment Type: Full-time
💰 Compensation not publicly listed. Market estimate for similar roles: from $80K, varying by experience and location.