DirecciónFrom LHH Life Sciences we are looking for a Clinical Research Manager for an important Research Institute.
Key Responsibilities
In liaison with the CMU coordinator and her team, the successful candidate will :
- Assist researchers in the management and coordination of clinical studies.
- Support in clinical protocols and informed consents development.
- Support on design / creation of study databases and EDCs (including REDCap)
- Organization and preparation of the required materials necessary to implement to the projects.
- Organization of & attendance to meetings, presentations, and minutes.
Requisitos Degree in the health fieldComplementary training / experience on clinical studies / trials management, including writing of clinical protocols and informed consent forms, will be appreciated.
Experience as CRA or similar will be valued.Experience in RedCAP databases / CRD design and management will be considered.
Writing skills, creativity and ability in design will be an asset. Good English level & high communication skills (written & oral).
Good organizational skills, excellent attention to detail and ability to plan and organize work.Initiative and ability to work in a multidisciplinary team.
Responsabilidades
Full-time job, stable positionHybrid work model (on-site + teleworking) subject to the foundations regulations.Immediate incorporationDynamic and highly collaborative unitAn international and interdisciplinary research environment consisting of wet lab scientists and data analysts.
Mixed basic and Clinical Research environment in BiomedicineTransversal and general training (such as gender equality, research seminars, scientific writing)State-of-the-art infrastructures and well-equipped offices / relaxing areas.
Generous vacation package : 22 vacation days, plus 4 days on Christmas, plus all long 3-day / 4-day weekends.Competitive salary.
