Job Overview
Location
Amsterdam HQ
Job Type
Full-time
Category
Data & Analytics
Date Posted
May 21, 2026
Full Job Description
đź“‹ Description
- • Lead the planning and execution of Real-World Data (RWD) collection within Expanded Access Programs (EAPs) and other non-interventional studies to support patient access to treatments in development.
- • Manage direct communication with clients, physicians, and site staff to ensure timely, accurate, and complete RWD collection across global study sites.
- • Monitor data quality in real-time, identify discrepancies, missing entries, or inconsistencies, and implement corrective actions to maintain high data integrity standards.
- • Ensure full compliance with ICH-GCP guidelines and other applicable regulatory requirements for RWD collection and documentation in non-interventional studies.
- • Refine, update, and maintain Standard Operating Procedures (SOPs), data collection templates, and study documentation to enhance efficiency and consistency across RWD programs.
- • Collaborate closely with Clinical Operations, Data Management, and Commercial teams to align RWD deliverables with program objectives and client expectations.
- • Track and report on key data quality and completion metrics for assigned programs, ensuring targets are consistently met or exceeded.
- • Act as a trusted point of contact for external stakeholders, building strong relationships with healthcare professionals and trial sites to facilitate smooth data flow.
- • Proactively identify opportunities to improve RWD processes, suggesting and implementing enhancements that increase accuracy, reduce delays, and improve overall data usability.
- • Maintain meticulous records of all data collection activities, communications, and compliance checks to support audits and regulatory inspections.
- • Contribute to the continuous improvement of myTomorrows’ RWD framework by sharing insights from field experience and participating in cross-functional process reviews.
- • Ensure all RWD activities are conducted with the highest ethical standards, prioritizing patient privacy and data security at every stage of collection.
- • Support onboarding of new sites and clients into RWD programs by providing clear guidance, training materials, and tailored documentation.
- • Participate in internal knowledge sharing sessions and contribute to the development of training content for new team members on RWD best practices.
- • Stay current with evolving regulatory guidance and industry standards related to Real-World Data and Expanded Access Programs to ensure myTomorrows remains at the forefront of compliance and innovation.
🎯 Requirements
- • Bachelor’s degree in Life Sciences, Pharmacy, or a related field
- • 2+ years of experience in Data Management, Real-world Data, or Clinical Research
- • Familiarity with electronic data capture (EDC) systems and strong proficiency in Microsoft Office Suite
- • Understanding of ICH-GCP guidelines (certification preferred)
- • Strong organizational and problem-solving skills with great attention to detail
- • Proactive, team-oriented mindset with a drive to contribute to myTomorrows' impact
🏖️ Benefits
- • Impactful work that helps patients gain access to potentially lifesaving treatments
- • Competitive salary, annual performance bonus, and an Employee Stock Option Plan
- • Attractive pension plan, with full premium covered by myTomorrows
- • Hybrid working model and policies to support working parents
- • Healthy lunch at the Amsterdam office
- • Unlimited access to professional guidance by certified psychologists via OpenUp
Skills & Technologies
Go
GCP
Hybrid
Degree Required
About myTomorrows B.V.
myTomorrows B.V. operates an Amsterdam-based platform that connects physicians and patients worldwide with pre-approval and off-label medicines. The company identifies investigational or licensed drugs not yet commercially available in a patient’s country, navigates regulatory pathways, arranges supply, and supports pharmacovigilance. It serves oncology, neurology, and rare diseases, working with pharmaceutical companies, hospitals, and regulators in Europe, North America, and Asia-Pacific.
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