Experienced Study Data Manager

il y a 1 semaine


Paris, France EBMT Temps plein

DESCRIPTION

**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.

**REQUIREMENTS**:

- ** 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)**:



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