- Study Start-Up Manager, SSU
Study Start-Up Manager/Project Manager with a Global CRO in Hungary, Budapest
- Submissions / Start Up Manager Budapest Hungary
Project Manager - Clinical Study Start-Up, Budapest, Hungary, JOB SUMMARYProject Manager for Clinical Study Start Up is required by a Global CRO, the role is office based in Budapest, Hungary. You will have worked for several years in Clinical Research and will be familiar with Study Start-up and Site Activation activities.
- ***Study Start up / Clinical Project Manager – Switzerland***
- Manager, Study Start-Up, EU
As a key member of our rapidly expanding global team at inVentiv Health Clinical, you will be responsible for managing employees within the Study Start-Up function across multiple regional and global projects.
As a Manager Study Start-Up, you will successfully ensure that your direct reports provide quality deliverables and achieve corporate and/or customer metrics and goals within GCP/ICH guidelines as well as applicable SOPs and policies.
- Manager, Study Start-up, Hungary or Russia
The position manages and is accountable for the work of professional level employees within the Study Start-up function.
- Country Study Manager - Stockholm - Start Up!
My client, a CRO in phase of start up in Sweden is currently looking for a Clinical Project Manager to join their team. The client is a CRO focused on the scientific quality of their studies as this is how they gained most of their business, hence you will find yourself in an environment where the quality of your work will be a strong priority
- Freelance Contracts Manager
My top Global client is looking for 2x Site contract managers to join their European team on a contract bases. - Developing procedures and training related with Start-up activities. - Managing project plans and timelines with regard to site contract in the designated region. - Serving as a project liaison to Sponsors and internal WCT Project Management teams to monitor study status, provide frequent region-specific metrics and status updates as needed. ...
- Freelance Clinical Study Manager, 6 Months
ROLE/DESCRIPTIONYou'll be managing European Clinical Cardiovascular Studies in Phase II. The emphasis of the role is study start-up and you will report to the global study lead. Responsibilities will include vendor (CRO) management, management of budget/timelines and review of relevant study documents to include protocols, informed consents, case report forms, monitoring plans, clinical study reports etc.
- Feasibility Manager (f/m) (based in the EMEA Region)
Feasibility Manager (f/m) (based in the EMEA Region)
Shared Work – Shared Vision: The way we do business, a promised standard that includes on-going support from a specialized team dedicated to meeting or exceeding our clients expectations.
Are you looking for a new challenge in a global and fast moving environment where your negotiating skills and attention to details are in demand? Then continue reading and join our growing company!
- Start-up/Regulatory Associate, Prague Czech Republic
Site Start Up and Regulatory Specialist (Global Role)Location: Office based - Prague, Czech RepublicSeveral roles with different level of seniority available. Please apply if you are a Start-up and/or Regulatory speacialist or CTA, Clinical Trial Coordinator, In-House CRA with experience in Submissions.