Study Coordinator
vor 2 Wochen
Title:
Study Coordinator
Company:
Global CRO
Location:
Fully on-site
- Hamburg
FTE:
0.5 FTE months contract
We are seeking a highly motivated and detail-oriented Clinical Study Coordinator to join our dynamic research team at one of Hamburg's premier university hospitals. You will play a pivotal role in administrative and technical support to the Project Team, and support audit readiness by ensuring files are reviewed on schedule detailed in the organization's WPD and department guidance document.
Key Responsibilities
- Provide administrative and technical support to the project team.
- Maintain and review study documentation to ensure audit readiness.
- Coordinate and complete clinical trial-related tasks based on assigned role (Central or Local).
- Support and maintain clinical trial systems (e.g., eTMF, GoBalto).
- Track regulatory documents and transmit to clients and ethics committees.
- Assist with scheduling meetings and distributing study materials.
- Analyze study metrics and help resolve documentation issues.
- Support Risk-Based Monitoring (RBM) and vendor tracking activities.
Qualifications
- Bachelor's or Master's degree in life sciences, nursing, pharmacy, or related field
- Several years of experience in clinical research or trial coordination
- Strong knowledge of GCP, ICH, and EU clinical trial regulations
- Excellent organizational and communication skills
- Proficiency in English and German (written and spoken)
- Experience with EDC systems and clinical trial management software is a plus
Interested? Apply now for immediate consideration or contact Maria Tsalpatourou at -
ABOUT PLANET PHARMA
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency.
We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
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