* You act as the primary point of contact for the study team and/or sponsor.
* You oversee study budgets and finances.
* You maintain study oversight through effective communication with key stakeholders.
* You manage project risks and resolve issues.
* You maintain oversight of eTMF and ensure high quality.
Your profile
* You have at least 4 years’ experience in clinical research and good knowledge of GCP.
HRA/REC submissions in the UK are an advantage, however full training will be provided.
* You have a life science degree or healthcare equivalent (Bachelor).
* You have strong communication skills and fluency in English.
* You are proactive.
* You are flexible when the role requires.
* You are great at prioritising and problem solving.
* You are organised, punctual, have great interpersonal skills and happy to work with the team.
* You have an entitlement to work in the UK.
* You have a UK drivers licence.
Why us?
* We ensure you a thorough introduction and support from a team of experienced natural scientists.
* We offer exciting and varied projects from the pharmaceutical, biotech and medical production sectors.
* We guarantee fast decision-making processes due to flat hierarchies and “open doors” culture.
* We love diversity! Our teams are diverse, cross-generational and we work and learn with and from each other.
* We have modern, well-equipped offices.
* We provide flexible home office options with a minimum of 2-3 days per week in the office.
Interested?
We are looking forward to your application.
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