Study Coordinator (m/f/d)

Gulp Ag; Biberach an der Riß; Vor Ort; EUR 42.000 - 62.000; Vollzeit

Zusammenfassung

GULP Information Services GmbH seeks a dedicated Study Coordinator (m/f/d) for a leading pharmaceutical company in Biberach. You will manage study logistics, coordinate the study team, and ensure quality data transfer.

Fluent German and good English required; nursing background and research experience are advantageous; you will support participants and interface with investigators.

Qualifikationen

• Nursing foundation: Completed training in health and nursing care, ideally with specialist training.
• Experience in research: practical experience as a study nurse or in the operational execution of clinical trials.
• Strong planning and empathetic, professional communication with study subjects and interfaces.
• Willingness to work study-related hours and plan assignments transparently as a team.
• Fluent German for daily interviews and good English for international study materials and SOPs.

Aufgaben

• Resource & Project Management: independently plan and coordinate all tasks for clinical trials, including personnel, logistics and equipment.
• Structure & Feasibility: create detailed schedules and source documents while monitoring feasibility across multiple projects.
• Support & Patient Care: assist study participants and support the principal investigator with non-medical tasks.
• Team coordination: provide technical guidance to the study team and ensure smooth daily workflow.
• Quality assurance & data: check study documents for quality and ensure error-free data transfer to sponsor databases.

Kenntnisse

Organization

Empathy

Team coordination

Flexibility

German language

English language

Ausbildung

Nursing foundation training

Jobbeschreibung

Ready for the next step? We make your job search easy: quick, straightforward, and direct to top positions. We are currently seeking a dedicated Study Coordinator (m/f/d) for a leading, nationally renowned research-based pharmaceutical company in Biberach. Immerse yourself in the world of clinical trials, take on responsibility at the interface of cutting-edge medicine, and strategically advance your career to the next level.

We are committed to equal opportunities and expressly welcome applications from people with disabilities.

Resource & Project Management

You will independently plan and coordinate everything necessary for the execution of clinical trials – from personnel and logistics to equipment.

Structure & Feasibility

You will create detailed schedules and source documents, keeping a close eye on feasibility even when multiple projects are running concurrently.

Support & Patient Care

You will support study participants and professionally assist the principal investigator with all non-medical tasks.

Team coordination

You will provide technical guidance to the study team and ensure a smooth and efficient daily workflow.

Quality assurance & data

You will check study-related documents for the highest quality and ensure error-free data transfer to the sponsor databases.

• Nursing foundation: Completed training in health and nursing care, ideally supplemented by specialist training (e.g. intensive care medicine or anesthesia).
• Experience in research: Practical experience as a study nurse or in the operational execution of clinical trials is a great plus for your entry.
• Organization & Empathy: You shine with a strong talent for planning and your empathetic, professional communication with test subjects and interfaces.
• Flexibility within the team: You are willing to work study-related hours – you plan your assignments transparently and together as a team.
• Language skills: Fluent German for daily interviews with study participants and good English for working with international study materials and SOPs.