Job description Project Manager CTS:
The PMs of CTS are capable to independently manage complex clinical research projects: phase I-IV, drugs, medical devices and food supplements.
Our PMs strive to complete their studies within the deadlines and according to the processes and conditions agreed upon. The project manager is responsible for the daily management of the trial.
Our PMs are trained and certified according to the International Project Management Association (IPMA). Our PMs are also extensively trained in ICH-GCP, Dutch law of medical-scientific research in humans and the European Clinical Trial Directive.
The CTS project manager communicates on a high and transparent level. The PM remains in close contact with all parties involved: sponsor, investigators, project team, laboratory, pharmacy, research centres etc., with regards to the progress and status of the trial.
The PMs of CTS are key to a successful conduct of the trial.
Main tasks/skills:
- Perform a feasibility check of the trial
- Identify the critical success and risk factors
- Complete the project within the timelines and budget agreed upon
- Manage the project organization
- Write a project plan
- Manage the project team
- Keep the project management system up to date
- Warrant the quality of the trial
- Make sure the trial is performed according to the Dutch and European laws and regulations
- Inform the sponsor of the most recent status of the project on predefined time points
- (Para-)medical background with a University or University of applied sciences degree
Want to become a PM at CTS? Apply!
Regularly vacancies!