Profil isan internationally renowned CRO in the field of metabolic diseases,founded in 1999. For many years, we have been working closely withthe pharmaceutical industry to develop new drugs for the treatmentof diabetes and related diseases. We also intensively support thefurther development of known active substances. Furthermore, weconduct vital research regarding various other excitingapplications such as novel routes of insulin administration or themeasurement of blood glucose concentrations. Our many years ofexperience have enabled us to build up comprehensive scientificknow-how and a unique expertise in the field of metabolic diseases.Profil currently employs around 330 people who make an importantcontribution to improving the quality of life of people withdiabetes.
This project manager will ensure thatclinical trials at PROFIL are conducted on time, within the plannedresources and with highest quality. Flexible working hours andmobile working will be possible as soon as the familiarisation andtraining into the new position is completed.
We are currently recruitinga
Project Manager(m / w / d)
Full-time
Your responsibilies :
- Plan project goals and objectives
- Responsible for project communication, coordination andcontrolling
- Demonstrate a goal-oriented,trusting, flexible and motivativing project work
- First point of contact for Sponsors, third-partyorganizations as well as internal interfaces
- Organize, lead and document Sponsor oversight meetingsand study handover meetings
- Schedule andfacilitate site-initiation visits
- Supportcross-departmental communication, problem solving anddecision-making
- Create Project ManagementPlans outlining tasks, milestones and required resources
- Maintain and control project timelines
- Report weekly project status updates
- Plan and coordinate clinical trial submissionpreparations
- Take responsibility for eTMFset-up and maintenance
- Manage project risksand issues
- Monitor project Key PerformanceIndicators
- Controlling of planned projecthours
- Controlling of project access rights andtraining requirements
Your profile :
ABachelor’s or an advanced degree in science (e.g. biology,chemistry etc) would be beneficialPreviousrelevant experience in a CRO is mandatory, as well as experience inclinical trial management and project managementEmpathetic, helpful personality who is proactive andfocused on solutions with a hands-on mentalityVery good MS-Office application skillsFluent English language skills are a must, Germanlanguage skills are a plusExceptionalorganizational and interpersonal skillsAbility to work both independently and within a teamsetting to obtain individual and company objectivesOur offer :
We take pride in our company culturebased on respectful, friendly and positive interactions between allcolleagues and between all levelsAn excitingrole with deep insights into clinical research at toplevelIn addition to flexible working hours,you can expect competitive pay with an annual salary increaseadjusted to the inlationIntensive inductioninto the job, comprehensive training on the job as well as theopportunity for further developmentBicycleleasing (also e-bikes) via the company Business Bike and freecharging possibility for ebikesPerformance-related pay with annual inflationcompensation and a secure job with a permanent employmentcontractAre youinterested in this role?
Don’t hesitate to sendus your CV, a motivation letter as well as records of yourqualifications / employment reference letters via email, preferablyas pdfs, to hr[AT]profil.com ( YF-15162 )
Profil Institut für StoffwechselforschungGmbH
Martin Schneider
ExecutiveDirector Human Resources
Hellersbergstraße9
41460 Neuss
www.profil.de