Act as the main point of contact for all data management topics and participate in project/study meetings
Contribute to the selection of subcontractors by preparing specifications and evaluating proposals
Participate in study design, including data management sections in protocols and CRF specifications
Oversee outsourced data management activities, ensuring compliance with cost, timelines, and data quality
Validate deliverables such as data management plans, validation plans, transfer specifications, eCRF completion guides, and coding instructions
Test eCRF before production deployment and after each protocol amendment
Implement targeted quality control of data based on risk assessment
Monitor progress of data management steps (entry, cleaning, coding, external data transfers, SAE reconciliation, etc.)
Regularly assess subcontractor service quality, establish action plans for deviations, and discuss corrective measures
Participate in data review meetings and validate associated reports
Ensure responsibility for database lock and unlock, verifying all prerequisites
Provide statisticians with data for statistical analysis
Verify the presence of all data management documentation in the Trial Master File (TMF)
Experience in clinical data management for CROs (5–10 years)
Proficiency with industry-standard data management tools and software
English fluent. French is a plus.
Act as the main point of contact for all data management topics and participate in project/study meetings
Contribute to the selection of subcontractors by preparing specifications and evaluating proposals
Participate in study design, including data management sections in protocols and CRF specifications
Oversee outsourced data management activities, ensuring compliance with cost, timelines, and data quality
Validate deliverables such as data management plans, validation plans, transfer specifications, eCRF completion guides, and coding instructions




Test eCRF before production deployment and after each protocol amendment

Implement targeted quality control of data based on risk assessment
Monitor progress of data management steps (entry, cleaning, coding, external data transfers, SAE reconciliation, etc.)
Regularly assess subcontractor service quality, establish action plans for deviations, and discuss corrective measures
Participate in data review meetings and validate associated reports
Ensure responsibility for database lock and unlock, verifying all prerequisites
Provide statisticians for data for statistical analysis
Verify the presence of all data management documentation in the Trial Master File (TMF)
Experience in clinical data management for CROs (5–10 years)
Proficiency with industry-standard data management tools and software
English fluent. French is a plus.
A robust training system with our internal Academy and 250+ available modules
Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support.
For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.
Amaris Consulting, part of Mantu is an independent technology consulting firm providing guidance and solutions to businesses.
With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries.
Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering.
Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.
Brief Call Our process typically begins with a brief virtual/phone conversation to get to know you! Case study Depending on the position, we may ask you to take a test.

📌 Clinical Data Manager (F/M/X) (Madrid)
🏢 Amaris Consulting
📍 Madrid