Project Manager Perm (m/f/d)

Rahmendaten

For a leading CRO the Project Manager&rsquo;s essential function is to organize and manage clinical studies, coordinating all involved departments as well as external vendors, and being the primary contact person for the sponsor.<br /> <br /> <strong>Focus of tasks:</strong><br /> - Set-up and conduct of clinical trials within applicable (local) laws, regulations and directives keeping scope, time, budget and quality within scope<br /> - Primary sponsor contact- Management and oversight of further involved parties including leading of national and international project teams, vendor management<br /> - Set-up and maintenance of timelines and tracking tools<br /> - Set-up and maintenance of trial specific plans and manuals<br /> - Set-up and maintenance of risk management<br /> - Interface support for e.g. protocol/ ICF development, feasibility/ site selection, EC/ regulatory submission, TMF maintenance, clinical monitoring- Oversight on study budget<br /> <br /> <strong>Profile:</strong><br /> - Degree in a scientific or medical discipline<br /> - At least 3 years of experience in the area of clinical trial management or clinical research, ideally multicenter and multinational trial experience<br /> - Strong organizational and communication skills<br /> - Well-structured and organized, target<br /> -oriented personality, team player<br /> - Very good English skills<br /> - Candidates with experiences in dermatology will be preferred<br /> &nbsp;