Job Description

Read job description in: German DE, English

Deine Aufgaben

• 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.

Dein Profil

• 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.

Warum wir?

• 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 ! Our teams are diverse, cross- 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.

Interessiert?

We are looking forward to your application.