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Data Analyst / Data Manager - Job Opportunity at Avania Clinical

Nederland, NL
Full-time
Mid-level
Posted: July 14, 2025
Hybrid
EUR 45,000 - 65,000 annually based on the Netherlands market for mid-level clinical data analysts with master's degree requirements, with potential for higher compensation given the specialized MedTech focus and global CRO environment

Benefits

Opportunity to work in an innovative, fast-growing and rewarding industry that positions professionals at the forefront of medical technology advancement
Access to a dynamic and enthusiastic global team fostering collaboration across multiple specialties, providing extensive networking and knowledge-sharing opportunities
Comprehensive knowledge exchange programs and career development initiatives backed by structured training opportunities, ensuring continuous professional growth
Competitive compensation and benefits package tailored to attract top talent in the clinical research sector
Travel opportunities for eligible roles, providing international exposure and cross-cultural professional experience
Flexible work arrangements including hybrid and fully remote options, supporting work-life balance and modern workforce preferences

Key Responsibilities

Lead protocol review and data management strategy development by analyzing study protocol data management sections to ensure regulatory compliance and operational efficiency
Architect comprehensive Data Management Plans that serve as the foundation for clinical trial data integrity and regulatory submission success
Design and develop Case Report Forms that optimize data collection processes and minimize site burden while ensuring complete data capture
Engineer and implement robust clinical databases that support multi-site global clinical trials and enable real-time data monitoring
Develop and program sophisticated data validation systems that ensure data quality and regulatory compliance throughout the trial lifecycle
Standardize data structures across therapeutic areas to enable efficient data analysis and regulatory submission preparation
Deliver comprehensive database training programs to hospital staff, ensuring proper data entry and site compliance
Execute advanced data review and cleaning processes that identify potential safety signals and ensure data integrity for regulatory submissions
Perform trend analysis and safety monitoring to support clinical decision-making and regulatory reporting requirements
Create and maintain interactive data visualization dashboards using enterprise tools like SAS and Power BI to support real-time trial monitoring
Manage client relationships and cross-functional collaboration to ensure project deliverables meet regulatory standards and timeline requirements
Oversee data analytics project timelines and deliverables while maintaining quality standards and regulatory compliance
Contribute to cross-functional initiatives with statisticians and medical writers to support comprehensive clinical trial reporting and regulatory submissions

Requirements

Education

Life sciences, Bio-informatics, Health Sciences, Human Movement Science, Computer Science, or other relevant master degree

Experience

Not specified

Required Skills

Proficient in the use of computer and software systems Experience with SAS, R, Power BI and/or any Clinical Database Management Software is a plus GCP, ICH-E6, and/or ISO14155 knowledge is a plus Accurate with strong attention to detail Excellent communication skills Team player with high energy and an ability to work independently or with a team Stress resilient Fluent in English

Certifications

GCP, ICH-E6, and/or ISO14155 knowledge is a plus
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Sauge AI Market Intelligence

Industry Trends

The clinical research industry is experiencing unprecedented growth driven by increased medical device innovation and regulatory modernization, with CROs expanding their data analytics capabilities to support complex multi-site global trials. Digital transformation in clinical trials is accelerating the demand for professionals who can bridge traditional data management with advanced analytics and visualization technologies. MedTech clinical trials are becoming increasingly data-intensive as regulatory bodies require more comprehensive real-world evidence and post-market surveillance, creating sustained demand for data analysts who understand both clinical operations and advanced analytics. The integration of artificial intelligence and machine learning in clinical data management is reshaping the role, requiring professionals to adapt to new technologies while maintaining regulatory compliance. The European clinical research market is experiencing consolidation among CROs, with mid-sized companies like Avania competing by offering specialized expertise in medical device trials and flexible work arrangements to attract top talent. Remote and hybrid work models have become permanent fixtures in the industry, enabling CROs to access global talent pools while maintaining operational efficiency.

Role Significance

The role involves working within a 15-person European data analytics team that is part of a larger 25-person global analytics organization, suggesting a collaborative environment with opportunities for mentorship and knowledge sharing across international markets
This is a mid-level position requiring advanced technical skills and independent decision-making capability, with significant responsibility for data integrity and regulatory compliance across global clinical trials. The role combines individual contributor responsibilities with client-facing activities and cross-functional collaboration, indicating a position that bridges technical execution with strategic business impact.

Key Projects

Multi-site international medical device clinical trials requiring complex data management and regulatory compliance Real-time safety monitoring and signal detection systems for ongoing clinical studies Regulatory submission preparation including data standardization and statistical analysis support Cross-functional collaboration on clinical study reports and regulatory documentation Implementation of advanced data visualization and analytics platforms for trial monitoring

Success Factors

Deep understanding of clinical trial regulations and data integrity requirements, particularly GCP and ICH-E6 guidelines, combined with practical experience in implementing compliant data management systems Proficiency in advanced analytics tools and programming languages, with the ability to translate complex clinical data requirements into technical solutions that support regulatory submissions Strong project management capabilities with demonstrated ability to manage multiple concurrent studies while maintaining quality standards and meeting aggressive regulatory timelines Exceptional attention to detail and quality assurance mindset, as data integrity issues can have significant regulatory and patient safety implications Effective communication skills for interfacing with clinical sites, regulatory authorities, and cross-functional teams across different time zones and cultural contexts

Market Demand

High demand driven by accelerating clinical trial activity, regulatory modernization, and the critical need for data integrity in medical device approvals

Important Skills

Critical Skills

Master's degree in life sciences or related field is essential as it provides the foundational knowledge of clinical research principles, regulatory requirements, and scientific methodology necessary for ensuring data integrity and regulatory compliance Attention to detail and accuracy are paramount in clinical data management, as errors can have serious regulatory consequences and impact patient safety, making these skills non-negotiable for success in the role Strong communication skills are critical for interfacing with clinical sites, regulatory authorities, and cross-functional teams, as data managers serve as key liaison points in the clinical trial process Stress resilience and ability to work independently are essential given the fast-paced, deadline-driven nature of clinical trials and the need to manage multiple concurrent studies with varying requirements

Beneficial Skills

Experience with SAS, R, and Power BI provides competitive advantage as the industry increasingly emphasizes advanced analytics and real-time data visualization for trial monitoring and decision-making GCP, ICH-E6, and ISO14155 knowledge, while listed as plus, becomes increasingly important for career advancement and demonstrates commitment to regulatory excellence Multilingual capabilities beyond English fluency can be valuable for international trials and European market operations Project management certification or experience enhances career prospects as data managers often progress to study management roles

Unique Aspects

Specialized focus on MedTech and medical device trials, which require different regulatory expertise compared to traditional pharmaceutical research and offer exposure to cutting-edge medical technologies
Opportunity to work with a relatively small, agile team while having access to global resources and international trial experience
Direct client interaction and cross-functional collaboration opportunities that are typically reserved for more senior roles in larger CROs
Combination of traditional data management responsibilities with advanced analytics and visualization work, providing broader skill development opportunities
Emphasis on training and development in a fast-growing company, suggesting accelerated career progression possibilities

Career Growth

Typical progression to senior roles within 3-5 years with demonstrated performance and additional certifications, with potential for leadership positions within 5-7 years

Potential Next Roles

Senior Data Manager or Lead Data Analyst with responsibility for managing junior staff and overseeing multiple therapeutic areas Clinical Data Science roles focusing on advanced analytics and machine learning applications in clinical research Regulatory Affairs positions leveraging data management expertise to support submission strategies Project Management roles overseeing entire clinical study operations Biostatistics positions combining data management background with advanced statistical analysis

Company Overview

Avania Clinical

Avania Clinical operates as a specialized contract research organization focusing on medical device and MedTech clinical trials, positioning itself as a boutique alternative to larger CROs with deep therapeutic expertise. The company's global footprint and emphasis on innovation suggests a growth-oriented organization that competes on specialized knowledge rather than scale alone.

Avania appears to be a mid-tier CRO that differentiates itself through specialized MedTech expertise and flexible work arrangements, competing with larger organizations by offering more personalized career development and direct client interaction opportunities
The Netherlands location provides access to the European clinical research market with proximity to key regulatory bodies and pharmaceutical companies, while the global team structure enables participation in international trials and cross-border collaboration
The emphasis on collaboration, innovation, and flexible work arrangements suggests a modern, employee-centric culture that values work-life balance while maintaining high performance standards in a regulated industry environment
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