Experienced 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 €41.470 gross per year (scale 13.0-13.3), 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)