Study Data Manager (Paris)

Are you looking for a job where you can make a difference and work in a non-profit? Would you like to be a part of an ambitious and international organisation on the cutting edge of science?  Then this position might be right up your alley.

The EBMT is a non-profit medical and scientific organisation which hosts a unique patient registry providing a pool of data to perform studies and assess new trends.

Our mission

Save and improve the lives of patients with blood-related disorders.

Your mission

Collect, enter, clean, report, and monitor data collection and contribute to the development and management of tools.

Responsibilities and Tasks

• Assist with reviewing study proposals/protocols, conducting feasibility studies, assessing the availability of data, need for additional data collection requirements, and potential bottlenecks for study conduct. 
• Create data questionnaires (CRF) or surveys and coordinate data collection with centers.
• Accurately enter information into a database and verify entries for accuracy and completeness . Ensure data quality and completeness by performing data quality checks.
• When needed generate queries and work with centers, and investigators and other data providers to discuss, clarify, and resolve data ambiguities, inconsistencies.
• Produce data sets, reports, charts, graphs, and tables for investigators, statisticians, managers, and other end-users.
• Possible contribution to the review of abstracts/manuscripts before submission. 
• Collaborate with other Data managers, Study coordinators, and Statisticians.

• Excellent written and oral communication skills in English.
• Graduated in biomedical sciences or related field (health engineering or physiology and data management or Masters degree in computer science with additional training in life sciences).
• At least 3-5 years of experience in study data management.
• Experienced user of Microsoft Office products, particularly Excel .
• Experience with large clinical databases.
• Knowledge of study data management principles and regulatory requirements for data processing.
• Basic knowledge of medical terminology.
• Ability to manage multiple activities effectively, and prioritize workload within timelines. Ability to communicate effectively with people in a multicultural/ multilingual environment. Team spirit, proactive attitude, flexible. Analytical thinking. Detail oriented.

Desirable

• Experience in CRO (Clinical Research Organization).
• Experience in Academic Research.
• Experience working with SPSS and with other statistical and programming software (R).
• Basic knowledge of statistics.

What we offer

• Be part of a non-profit society where you can make a difference
• Work alongside a multicultural and diverse international team
• First-year with CDD contract. Possibility to have a CDI after 1-year commitment
• Flexible schedule (starting from 8 to 10 am and finishing accordingly)
• Full-time contract, 37.5 working hours per week
• 25 working days of Annual leave + 15 days RTT
• Salary range between €37.849 to €42.753 gross per year (scale 13.0-13.4), depending on previous experience.

Additional benefits

• Transport allowance (Forfait mensuel NAVIGO Toutes Zones)
• After the probation period, EBMT supports nursery costs with a monthly supplement
• Some days work from home and some days from the office (minimum 2 days at the office), although during the training period, you will be mostly at the office.
• After 1 year of work with us, you will receive a one-off payment of 800 euros gross to help you set up your home office.

Location (Hybrid)

Please note: we do not sponsor visas.

To support fair and unbiased recruitment, we also encourage candidates to remove personal details such as name, age, gender, or other identifying information from their CVs if they prefer.

Please submit your CV in English.