Location: Remote, with initial handover at site in Bracknell
Contract length: 6 months from start
Duties
Work under supervision of Product Safety experts to deliver the following accountabilities:
- Support with data entry and accuracy checks for a key internal database
- Engage with Global PLCM team and IT development teams to resolve challenges
Skills
- Ability to work independently under moderate level of guidance and direction
- Reliable and trustworthy, attentive to details
- Patience and concentration
- Experience working successfully in a multidisciplinary team environment
Education
- BSc in Natural Science
- Knowledge on data management is preferable, basic familiarity with the concept of databases
- Knowledge of Product Safety terminology and core areas (Toxicology, Consumer Safety, Environmental Safety)
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Scientific Data Adminstrator in Bracknell employer: SRG
As a Senior Clinical Trial Manager at our company, you will thrive in a dynamic and collaborative work environment that prioritises innovation and employee development. We offer competitive benefits, a strong focus on professional growth, and the opportunity to work alongside industry leaders in a location renowned for its commitment to advancing clinical research. Join us to make a meaningful impact in the field of clinical trials while enjoying a supportive culture that values your contributions.
