Your mission
- 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 develop appropriate study management plans.
- You manage project risks and resolve issues.
- You review monitoring visit reports.
- 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.
We invite you to join us in making a lasting difference in the lives of countless patients. Every day anew.
Interested?
We are looking forward to your application.