- 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.
- Study Start-Up Manager, SSU
Study Start-Up Manager/Project Manager with a Global CRO in Hungary, Budapest
- Regulatory Affairs Manager\Regulatory Affairs Project Manager
Regulatory Affairs Manager\Regulatory Affairs Project Manager
We are working in partnership with a global CRO, who are currently looking to fill four Regulatory Affairs Managers/ Regulatory Affairs Project Manager positions to work from their Surrey office or work from home. This company is recognised around the globe as the leader in clinical research and specialises in a wide range of therapeutic areas, including Paediatrics, Oncology and Immunology.
- 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.
- 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!
- 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.
- Regulatory Submissions Manager – UK, Germany, The Netherlands, Belgium & Hungary
Just Pharma are currently working on behalf of a rapidly expanding organisation within the Pharmaceutical sector looking for an experienced Study Start-up/ Regulatory Submissions professional to join their Clinical Operations team.
- Clinical and Regulatory Start-up Lead - UK
Premier Research are a growing global CRO focused on delivering high quality clinical research projects to their diverse client base. With industry leading expertise in Paediatrics, Analgesia, Oncology and CNS we are looking for career focused individuals who want to be a part of our growth
- Clinical and Regulatory Start-up Lead - Europe
Premier Research are a growing global CRO focused on delivering high quality clinical research projects to their diverse client base. With industry leading expertise in Paediatrics, Analgesia, Oncology and CNS we are looking for career focused individuals who want to be a part of our growth.