- 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.
- ***Study Start up / Clinical Project Manager – Switzerland***
- 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 Manager, SSU
Study Start-Up Manager/Project Manager with a Global CRO in Hungary, Budapest
- 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. ...
- PW 6275 Clinical Project Manager
An excellent opportunity for an experienced Clinical Project Manager to contribute to the European set up of global phase III studies for a small, innovative, specialist biopharmaceutical organisation. This role will encompass having full oversight of all EU components ideally suited to candidates who have worked up to management level, fully responsible for budgets, timelines and full CRO/ vendor management.
- 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.
- Global Study Start-up (GSSU) Specialist II - France - Contract
inVentiv Health Clinical are currently seeking a Global Study Start- Up Specialist II to join our company in Spain. This is an exciting permanent opportunity and you will be focused on regulatory Institutional Review Board (IRB) and Ethics Committee (ED) processes and documentation requirements for the start-up and conduct of clinical trials according to Good Clinical Practice and local regulations. A Global Study Start Up Specialist may be assigned to more than one project.
- Clinical Study manager- Epidemiology
Clinical Study manager- Epidemiology 6 month contract position
Location: Buckinghamshire, High Wycombe, London, Surrey, Hampshire
Competitive daily rate. Working Within a specialist Talented Epidemiology team
Are you an experienced Clinical Study manager within the specialist Epidemiology field? I have a 6 month maternity cover contract available to begin immediately- Negotiable day rate opportunity.
- CRAII - SCRA - Hungary - Home or Office Based
CRAII - SCRA required for an exciting new position with a Global, Medium CRO. If you are a Clinical Research Associate with 12 months+ experience and looking for a new challenge you can be rewarded with a generous salary and benefits package, flexible working arrangements and unequalled training and career development opportunities. We are looking for someone who is office or home based in Budapest, Hungary.