Data manager / IT Developer – CSV in clinical research

About the company

At QIMA, our daily mission is to provide services that enable our clients to prove the compliance and effectiveness of their products.

Present in more than 100 countries, we serve the consumer goods, food, and life sciences industries and help more than 30,000 brands, retailers, manufacturers, and producers achieve excellence in quality.

We combine field expertise, digital solutions, and scientific research to ensure compliant and reliable data for our clients.

Our 6,000 employees work every day according to our values. With customer passion, integrity, and a commitment to simplifying processes, we have transformed the Testing, Inspection, and Certification industry.

QIMA Life Sciences supports world leaders in the pharmaceutical, biotechnology, and cosmetics industries through an offering of scientifically validated tests and preclinical and clinical models.

Our solutions allow, from the very first stages, the identification of the most promising drug candidates, formulas, or active ingredients. They thus contribute to optimizing resources, accelerating development, and improving success rates.

As a trusted partner, our scientific expertise allows us to provide our clients with robust data, essential for informed decision-making and the development of innovation.

Your tasks

As a Data Manager / IT Developer – CSV in clinical research, your mission consists of managing clinical data and developing IT solutions compliant with regulatory requirements.

Interactions: Close collaboration with Project Managers, TEC, Quality, and the medical team

_Data management_

• Ensure the design and administration of study databases: eCRF, consistency checks, queries, database lock
• Guarantee the quality, consistency, and traceability of clinical trial data: implementation of controls, documentation

_Interface with Group IT_

• Ensure liaison with Group IT: deployment, maintenance, security
• Manage the secure server environment and access to internal resources
• Ensure the technical compliance of infrastructures

Additional missions Development of software modules for clinical research

• Develop data collection systems from a legacy system
• Gather requirements in cooperation with operational teams
• Explore and integrate AI solutions: automation, document extraction and structuring, decision support
• Document and validate developed solutions (specifications, tests) according to GAMP 5 and 21 CFR Part 11
• Mobilize your knowledge in computerized system validation (CSV)

Requirements

Hard skills

• Bachelor's to Master's degree in computer science, development, or data science
• Proficiency in PHP, jQuery, and SQL
• Knowledge of generative AI: integration of LLM APIs and automation
• Ability to organize documentation and archiving in an audited environment
• Excellent communication skills in English, both written and oral

Soft skills

• High autonomy
• Rigor and organizational skills
• Curiosity
• Proactivity
• Ability to propose solutions
• Strong entrepreneurial spirit
• Good interpersonal skills

What we offer

Remuneration

• Remuneration €32,000 gross annual for 39h per week

Other

Contract

• Offer: CDI, full-time
• Working time: 39h00 per week (35h00 + 4h00 additional)
• Job location: Nice
• Availability: early December 2026 or January 2027