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Data Analyst / Data Manager - Job Opportunity at Avania Clinical

Nederland, NL
Full-time
Entry-level
Posted: July 12, 2025
Hybrid
EUR 45,000 - 60,000 per year based on Netherlands market rates for entry to mid-level data analyst positions in clinical research, with potential for higher compensation given the specialized MedTech focus and global company scope

Benefits

Opportunity to work in an innovative, fast-growing and rewarding industry that positions professionals at the forefront of medical device development
Access to a dynamic and enthusiastic global team fostering collaboration across multiple specialties, providing extensive networking and learning opportunities
Structured knowledge exchange programs and career advancement support backed by comprehensive training and development opportunities that accelerate professional growth
Competitive compensation and benefits package designed to attract and retain top talent in the clinical research industry
Travel opportunities for select roles, providing international exposure and broader industry experience
Flexible work arrangements including hybrid and fully remote options, supporting work-life balance and attracting global talent

Key Responsibilities

Lead strategic review and analysis of study protocol data management sections to ensure regulatory compliance and operational excellence
Develop comprehensive Data Management Plans that serve as the foundation for successful clinical trial execution
Design and architect Case Report Forms based on study protocols, directly impacting data quality and trial efficiency
Build and optimize databases for clinical study data collection, ensuring scalability and regulatory compliance
Implement sophisticated data validation checks and standardization processes that minimize errors and accelerate trial timelines
Deliver critical database training to hospital staff, ensuring proper data collection and protocol adherence
Execute comprehensive data review and cleaning processes that directly impact trial integrity and regulatory submissions
Identify critical data trends and safety concerns that inform key medical device development decisions
Create and program advanced data visualization dashboards using SAS and Power BI to support executive decision-making
Manage strategic client communications and cross-functional collaboration to ensure project success
Drive data analytics project deliverables and timeline management, directly impacting company profitability and client satisfaction
Contribute to high-impact cross-functional initiatives with statisticians and medical writers that shape product development outcomes

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, not a requirement GCP, ICH-E6, and/or ISO14155 knowledge is a plus, not a requirement 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, not a requirement
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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 focus on real-world evidence, creating substantial demand for skilled data analysts who can bridge the gap between traditional pharmaceutical research and emerging MedTech solutions. This convergence is particularly significant as medical devices require specialized data management approaches that differ from traditional drug trials. Digital transformation in clinical trials is accelerating the adoption of advanced analytics platforms and cloud-based data management systems, with companies increasingly seeking professionals who can implement sophisticated data visualization and predictive analytics capabilities to improve trial efficiency and regulatory submission quality. The European medical device regulatory landscape has become increasingly complex following the implementation of MDR (Medical Device Regulation), creating heightened demand for data management professionals with specific expertise in medical device clinical trials and regulatory compliance frameworks. Remote and hybrid work models have become permanent fixtures in the clinical research industry, enabling companies to access global talent pools and creating opportunities for professionals to work on international projects without geographical constraints, fundamentally reshaping career development paths in the field.

Role Significance

Part of a 15-person European data analytics team within a larger global team of 25 professionals, indicating a substantial organizational commitment to data analytics and providing extensive peer learning and collaboration opportunities
This is a mid-level individual contributor role with significant strategic impact, offering substantial autonomy in data management decisions while providing clear pathways for advancement into senior data science or project management positions within the clinical research hierarchy

Key Projects

Leading end-to-end data management for Phase II and Phase III medical device clinical trials with multi-site international scope Implementing advanced data analytics solutions for real-world evidence studies that support regulatory submissions to EMA and FDA Developing comprehensive data visualization platforms that support executive decision-making for product development strategies Managing cross-functional initiatives that integrate statistical analysis, medical writing, and regulatory affairs to accelerate time-to-market for innovative medical devices

Success Factors

Developing deep expertise in medical device regulatory frameworks and clinical trial methodologies will be crucial for long-term success, as this specialized knowledge commands premium compensation and opens doors to senior regulatory affairs and clinical development roles Building strong relationships with global team members and external stakeholders, including clinical sites and regulatory authorities, will be essential for career advancement and project success in this highly collaborative environment Maintaining current knowledge of emerging data analytics technologies and regulatory requirements will be critical as the industry undergoes rapid digital transformation and regulatory evolution Demonstrating ability to translate complex clinical data into actionable business insights will distinguish high-performing professionals and create opportunities for advancement into strategic roles

Market Demand

High demand driven by the expanding medical device industry, increasing regulatory requirements, and the growing emphasis on data-driven decision making in clinical research

Important Skills

Critical Skills

Strong analytical and technical skills are fundamental for success in this role, as the ability to design, implement, and maintain complex clinical databases directly impacts trial success and regulatory compliance. Proficiency in statistical software and database management systems will determine efficiency and advancement potential. Exceptional attention to detail and accuracy are non-negotiable requirements in clinical data management, where errors can have significant regulatory and financial consequences. The ability to maintain precision under pressure while managing multiple complex projects simultaneously is essential for professional credibility. Communication and collaboration skills are crucial for success in this highly interdisciplinary environment, where effective interaction with clinical sites, regulatory authorities, and internal stakeholders directly impacts project outcomes and career advancement opportunities.

Beneficial Skills

Regulatory knowledge in GCP, ICH-E6, and ISO14155 provides significant competitive advantage and accelerates career progression into senior regulatory roles, particularly valuable given the increasing complexity of medical device regulations Advanced data visualization and analytics capabilities using tools like SAS, R, and Power BI will become increasingly important as the industry emphasizes data-driven decision making and real-world evidence generation Project management and leadership skills will be essential for advancement into senior roles, as the ability to coordinate complex clinical trials and manage cross-functional teams becomes increasingly valuable in the expanding clinical research market

Unique Aspects

Specialized focus on medical device clinical trials provides unique expertise that is increasingly valuable as the MedTech industry expands and regulatory requirements become more sophisticated
Global team structure with significant European presence offers international career development opportunities and exposure to diverse regulatory environments
Emphasis on advanced analytics and data visualization capabilities positions the role at the forefront of industry digitalization trends
Cross-functional collaboration with statisticians and medical writers provides comprehensive exposure to clinical development processes and enhances career versatility

Career Growth

Typical progression to senior roles within 2-3 years given the high-growth environment and expanding industry demand, with potential for accelerated advancement based on performance and additional certifications

Potential Next Roles

Senior Data Manager with expanded responsibility for multiple concurrent studies and team leadership Clinical Data Science Lead focusing on advanced analytics and predictive modeling for medical device development Regulatory Affairs Specialist leveraging data management expertise to support regulatory submissions and agency interactions Project Management roles in clinical operations, utilizing data management background to oversee comprehensive trial execution

Company Overview

Avania Clinical

Avania Clinical operates as a specialized contract research organization with a focused expertise in medical device and MedTech solutions, positioning itself in the high-growth intersection of clinical research and medical technology innovation. The company's global footprint and diverse therapeutic area coverage indicate a well-established market presence with significant growth trajectory.

Positioned as a leading player in the specialized MedTech CRO market, competing with established organizations like IQVIA and Syneos Health while maintaining competitive advantages through specialized expertise and agile organizational structure
The Netherlands location provides strategic access to European pharmaceutical and medical device markets, with proximity to major regulatory bodies and pharmaceutical hubs, while the global team structure offers international career development opportunities
Fast-paced, growth-oriented environment that emphasizes innovation and collaboration, typical of successful CRO organizations that must balance scientific rigor with commercial efficiency and client service excellence
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