inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing from a single clinical professional to an entire functional team.
Performs assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials. Responsible for providing delivery and expertise in one or more of the following functional areas: investigator site contracts, ethics and regulatory submissions, and review and finalization of essential documents required for site initiation.
Performs assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials. Responsible for providing delivery and expertise in one or more of the following functional areas: investigator site contracts, ethics and regulatory submissions, and review and finalization of essential documents required for site initiation.
This is an exciting role with one of the industry leading CROs. This is an office-based role in London. 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.
This is an exciting role with one of the industry leading CROs. This is an office-based role in London. 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.
Study Start-up Specialist / Regulatory Affairs Associate required to join a leading international CRO who are developing their Clinical & Regulatory Affairs team throughout Europe. This is a permanent position and can be office based in Munich or home based anywhere in Germany.
This is an exciting role with one of the industry leading CROs. This is an office-based role in London. 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 Clinical Research or Study Start-Up.
BENEFITS - Generous Salary - Full Benefits Package (Pension Scheme, Private Healthcare, Life Assurance etc.)
A Global Study Manager required by global CRO. You'll be working with a recognised global leader in the sector and will enjoy excellent ongoing career developmet opportunities to work towards Associate Project Director level. You must have full-service global Project Management experience gained within a CRO environment. Locations for this role include: UK, Spain, Germany, Italy, Belgium , Netherlands, France, Poland , Romania , Hungary and Czech Republic
A Global Study Manager required by global CRO. You'll be working with a recognised global leader in the sector and will enjoy excellent ongoing career developmet opportunities to work towards Associate Project Director level. You must have full-service global Project Management experience gained within a CRO environment. Locations for this role include: UK, Spain, Germany, Italy, Belgium , Netherlands, France, Poland , Romania and Czech Republic
A Global Study Manager required by global CRO. You'll be working with a recognised global leader in the sector and will enjoy excellent ongoing career developmet opportunities to work towards Associate Project Director level. You must have full-service global Project Management experience gained within a CRO environment. ...
Pharmiweb.com RSS Feeds 
PharmiWeb Candidate Blog
