Clinical Data Manager (F/M/X)

Amaris Consulting

Lyon

On-site

EUR 50,000 - 70,000

Full time

14 days+

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Benefits offered by this job

International community with diverse nationalities
Robust training and development system
Vibrant workplace culture with internal events
Opportunities to lead impactful sustainability projects

Job summary

A dynamic consulting firm located in France is hiring a Data Manager to oversee clinical data management activities within CRO environments. The candidate will ensure quality and compliance for clinical projects, supervise outsourced data management, and engage in study design. Proficiency in industry-standard data management tools along with a background in Life Sciences is required. Join a vibrant community focused on sustainability and diversity.

Qualifications

  • 5–10 years of experience in clinical data management for CROs.
  • Proficiency with industry-standard data management tools.
  • Fluent in English; French is a plus.

Responsibilities

  • Supervise data management activities for clinical projects.
  • Act as the main contact for all data management topics.
  • Ensure compliance with cost, timelines, and data quality.

Skills

Clinical data management
Analytical skills
Problem-solving skills
Fluent English
Knowledge of data management tools

Education

Academic background in Life Sciences, Pharmacy, or related field

Tools

Industry-standard data management tools and software

Job description

Amaris is looking for a Data Manager with strong experience in clinical data management for CRO environments. The position focuses on supervising data management activities to ensure the smooth progress and quality of clinical projects.

  • 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.)
  • Approve SDTM specifications and verify SDTM packages as needed
  • 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
  • Academic background in Life Sciences, Pharmacy, or related field
  • English fluent. French is a plus.
  • You demonstrate strong analytical and problem-solving skills
💡 What You’ll Get From Us
  • An international community bringing together 110+ different nationalities
  • An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities
  • A robust training system with our internal Academy and 250+ available modules
  • A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.)
  • At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. 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.

Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. 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.

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