Company: i-Pharm Consulting
Closing Date: 25 Oct 16
Salary (£): Negotiable
A global CRO is looking for an ambitious Manager Study Start Up with regulatory submission experience in Italy. As a Study Start Up Specialist you will be responsible for the management of the regulatory processes and the documentation for the overall start up activity.JOBTITLE Manager Study Start Up LOCATION Italy – Lombardia – Office BasedBENEFITS Generous Salary Full Benefits Package Industry leading training programmes with excellent ongoing career progression opportunities. ...
A global CRO is looking for an ambitious Manager Study Start Up with regulatory submission experience in Italy. As a Study Start Up Specialist you will be responsible for the management of the regulatory processes and the documentation for the overall start up activity.
Manager Study Start Up
Italy – Lombardia – Office Based
Full Benefits Package
Industry leading training programmes with excellent ongoing career progression opportunities.
To review and negotiate all regulatory documents for completeness, to negotiate with investigators, research nurses and site staff where necessary.
Able to identify activities along the critical pathway towards the start-up and completion for a study
Work with clinical research associates to ensure documents are collected and submissions occur.
Life Sciences Degree or equivalent, in a scientific or healthcare discipline
2 years + Regulatory Submissions
Experience working in a CRO or Pharma Company
Fluency in Italian and English
Line Management Experience preferred
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
If you would like to discuss this vacancy further, please call Principal Consultant Chiara Zentile on +39 02 94752015, or email firstname.lastname@example.org. If this role is not suitable, Chiara is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
CRA / CRAI / CRA II / SSU / Senior CRA / SCRA / Senior Clinical Research Associate / Lead CRA / LCRA / Monitoring /Monitor / Clinical Trial / Drug Trial / Trial Sites / Clinical / CRA 1 /CRA 2 / ICH-GCP / Clinical Research / Clinical Trials / Study Start-Up / Start-Up / Study Start Up / SSU / Clinical Study Start-Up/ Regulatory Affairs / Regulatory Documents / ICH-GCP / Central Europe / Eastern Europe / SCRA / Clinical / Home Based / Office Based/ Milan/ Rome/ Venezia/ Firenze/ Ancona/ Padova/ Torino/ Alessandria/ Asti/ Cuneo/ Novara/ Vercelli/ Parma/ Monza/ Arezzo/ Cagliari/ Olbia/ Napoli/ Bari/ Lecce/ Brindisi/ Caserta/
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