As an EDC Data Solution Specialist (Data Manager), you will work at the intersection of data, systems, and clinical research. You will translate clinical study requirements into practical EDC solutions — from understanding study protocols to building and testing electronic forms, configuring validation rules, and supporting clinical data throughout the study lifecycle.
We are looking for someone with a strong analytical mindset and relevant experience working with data, software systems, or structured technical processes. Previous experience with EDC systems or clinical trials is an advantage, but not a requirement. You will receive training on our EDC platform and study-specific processes.
• Review clinical study protocols and translate their requirements into electronic case report forms (eCRFs) and system configurations
• Build, configure, test, and maintain clinical study databases in the EDC system
• Configure forms, edit checks, validation rules, workflows, and study-specific functionality
• Test configured solutions and verify that data is collected and processed according to study requirements
• Create and maintain database specifications, validation guidelines, and other study documentation
• Investigate data discrepancies and support query generation and resolution
• Import, verify, and reconcile laboratory, safety, and other external study data
• Prepare study datasets and support data exports, database lock/unlock, and archiving
• Work with customers and internal teams to understand requirements and resolve system- and data-related questions
• Contribute to EDC procedures, guidelines, templates, and documentation
• Support EDC users and develop your expertise in clinical data flows and EDC processes
• You have a university degree in Computer Science, Life Sciences, Medical Sciences, or a related field
• You have relevant professional experience working with data, software systems, system implementation/configuration, business or system analysis, or other structured technical processes
• You are comfortable working with data structures, validation logic, data quality, and data flows
• You can analyze requirements and translate them into clear and structured solutions
• You have strong analytical and problem-solving skills
• You are detail-oriented and able to identify inconsistencies, errors, and gaps
• You are comfortable learning new technical systems and understanding how their components and processes work
• You can work independently while collaborating effectively with colleagues and customers
• You communicate confidently in English, both written and spoken
• Experience with EDC or other clinical/medical software systems
• Experience in clinical trials or clinical data management
• Previous experience with system configuration, form builders, workflows, validation rules, or similar tools
• Experience with eCRFs or IRT
• Knowledge of MedDRA or WHO Drug
• Understanding of clinical trial data flows, data validation, reconciliation, or database lock processes
Job conditions:
• Flexible work schedule
• Fully remote
• Annual leave (depends on contract type)
• Sick days fully paid by the company (depends on contract type)
• Competitive compensation depending on experience and skills
• Awesome team of highly qualified professionals
• Open door policy; low bureaucracy level
How we work:
• We care more about the things you do rather than your set working hours. We have flexible start hours from 8:00 to 11:00. Participating in meetings with clients and (fixed) team meetings is important.
• We value respect, transparency, proactivity, openness, and a positive approach. We care about our team’s mental health and happiness, which is why we follow an open-door policy and accept constructive feedback from both sides.
• We believe in teamwork with our clients and employees and build long-lasting, trusted relationships.
To apply for this position, please contact:
Originally posted on Himalayas