A dynamic global CRO is looking for a Study Start â€“ Up Manager to join their Clinical Operations team and to manage European-wide, clinical trial application submissions and overall start up processes. The position is office based in Munich.
Regulatory Affairs Manager\Project Manager
Permanent - Home-based or Surrey
We are working in partnership with a global CRO, who is seeking to fill positions for four Regulatory Affairs Managers/ Regulatory Affairs Project Managers to either be based in their office in Surrey, or home-based if Surrey is not a commutable distance. This company is recognised around the globe as the leader in clinical research...
This is an exciting role with one of the industry leading CROs. This is an office-based role in Madrid. This role is for someone with healthy experience in Clinical Research that has a strong interest in submissions and feasibilities. You will have an experienced background in Regulatory Affairs, Clinical Research or Study Start-Up.
Senior Study Start Up Associate/Regulatory Specialist: This CRO is continuing its expansion in Europe following a some great business wins and they are currently looking for a Regulatory Affairs Specialist to join their team in the M4 corridor. You will be covering CTAs across a range of therapeutic areas. Ideal for someone with strong experience in regulatory submissions looking to gain experience at a slightly smaller CRO with a great team atmosphere and company culture.
Regulatory Submissions Manager required to join a successful specialist CRO in Belgium on a permanent basis. This is an office based position close to Brussels and my client is offering an excellent salary, benefits package and career progression.
As the successful candidate you will be responsible for planning and facilitating global study start-up process. You will compile study start-up documents specifically related to Institutional Review Board and/or Ethics Committee (EC) submissions per country regulations. You will coordinate site identification and site contracting activities and act as primary point of contact for GSSU.
My client a market leading global CRO is currently growing it's regulatory & SSU division in it's UK head office. It is looking for experienced & knowledgeable regulatory professionals to join the team. If you are keen to progress into a full regulatory project management level role, leading global project teams in an exciting & dynamic environment then this is the opportunity for you!
Study Start Up Associate/Specialist: This CRO is continuing its expansion in Europe following a great 2013 and they are currently looking for a Study Start Up Associate to join their team in South East England. You will be covering MHRA and EC submissions across a range of therapeutic areas. Ideal for a Start Up Associate with strong experience in regulatory submissions looking to gain experience at a slightly smaller CRO with a great team atmosphere and company culture.
As a Global Study Start Up Specialist you will act as a local specialist regarding 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. At times you may also have the opportunity to be involved with startup activities for multiple countries.
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