Stellendetails zu: Projectmanager International -Clinical Project Manager" or "Clinical Trial Manager" (m/w/d)
Projectmanager International -Clinical Project Manager" or "Clinical Trial Manager" (m/w/d)
Projectmanager International -Clinical Project Manager" or "Clinical Trial Manager" (m/w/d)
Kopfbereich
Besondere Merkmale
- Homeoffice möglich
Arbeitsort
BremenAnstellungsart
Vollzeit, Teilzeit (Vormittag, Nachmittag)Beginn
ab sofortBerufsbezeichnung
- Director Regulatory Affairs (Pharma/Life Science)
- Biochemiker/in
- Pharmazeut/in
Stellenbeschreibung
International Project Manager
We are expanding our team and are looking for a proactive, dynamic** Project Manager** who wants to join a creative and motivated team of Project Managers. Our Project Managers should be team players with a strong service provider and leadership attitude. We are looking for people who love to work with modern software, to solve problems and who are willing to learn continuously. In this context, we are looking for a candidate who understands the importance of the following:
- Taking responsibility for steering the clinical studies through all expected and unexpected milestones
- keep the oversight of study risks, budget, timelines, vendors and streamline the work and results of international teams
- Having the confidence to present study status, issues and solution in front of clients
- Being able to think outside the box and finding creative solutions
Your profile:
- At least 3-5 years of experience in clinical research, preferably in a CRO
- Excellent communication and self-management skills
- Business fluent level in spoken and written English (and German preferred).
- Experience in Project Management or taking over Project Leadership
- Englisch C1 required
We offer:
- An independent, diverse and interesting area of responsibilities and an excellent working environment
- A dynamic team which likes to work together with passionate people who enjoy valuable work
- A young company culture and management, with a clear path to personal development and the opportunity to take responsibility not only within projects, but also within the company
- Flexible working hours with the possibility for home office
- A CRO caring to enable investigator initiated research by taking over sponsorship
Interested? An extremely innovative company is waiting for you. The salary will depend on your experience, performance, and value you will bring to our clients. If you are interested, send us your application to: hr@gcp-service.com
Arbeitsorte
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