Clinical Project Manager (m/f/d)

Gulp Ag; Hamburg; On-site; EUR 42,000 - 65,000; Full time

Job summary

Randstad in Hamburg is seeking a dedicated study coordinator to lead planning, management, and development of complex study designs within a scientifically demanding environment. You will advise internal departments on study parameters and regional coordination of global projects, organize and conduct human subject studies using biophysical measurements, and liaise with external testing institutes.

You will perform data control, prepare study reports, and present results clearly, while

Qualifications

• Completed studies in a natural science or comparable qualification.
• Relevant experience in cosmetic or clinical product studies or formulation development is preferred.
• Solid knowledge of writing study reports and ideally in-vivo efficacy and tolerability testing.

Responsibilities

• Plan, manage, and develop complex study designs independently and proactively.
• Advise internal departments on defining targeted study parameters and regional coordination of global projects.
• Organize and conduct human subject studies using biophysical measurement methods and clinical assessments, including liaising with external testing institutes.
• Perform independent data checks and prepare study reports with clear presentation of results.
• Participate in claim kick-offs and approval processes.

Skills

German fluency

English fluency

Project coordination

Communication skills

Independent work style

Education

Natural sciences degree or equivalent

Tools

MS Office

Job description

Are you looking for a new professional challenge in Hamburg and have a strong passion for clinical research? Our specialists at Randstad will guide you on your career path and help you find a position that perfectly matches your profile. As a dedicated study coordinator, you will be the interface in a scientifically demanding environment. We value diversity and welcome all applications, as equal opportunities are a core part of our philosophy. Your responsibilities will include: independent and proactive planning, management, and further development of complex study designs; advising internal departments on defining targeted study parameters and regional coordination of global projects; organizing and conducting human subject studies using biophysical measurement methods and clinical assessments, including liaising with external testing institutes; independent data control, preparation of study reports, and clear presentation of results; and active participation in claim kick-offs and approval processes.

• Completed studies in a natural science (e.g., pharmacy, cosmetics, chemistry) or a comparable qualification
• Relevant professional experience in conducting cosmetic or clinical product studies or in formulation development
• Solid knowledge of writing study reports and ideally experience with in-vivo efficacy and tolerability testing.
• Fluent German and English skills, as well as proficient use of standard MS Office applications.
• Independent, structured work style combined with strong communication skills and team spirit