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Clinical Project Director (Phase II and III) UK/EU

This job is no longer available

Employer
I-Pharm Consulting Ltd
Posted
Thursday, August 02, 2012
Closes
Thursday, August 30, 2012
Ref
NTHL00143
Contact
Natalie Hall
Location
England
Contract Type
Permanent
Hours
Salary
GBP0.00 per annum

Further information


Clinical Project Director - Top 5 CRO / Phase II and III


OVERVIEW

As a Clinical Project Director you will responsible for directing, supervising and managing large, global, complex, multi-regional, projects or multi-project programs. This role would also have strategic decision-making responsibility for the project. Some will involve line-management responsibilities. This position offers competitive salary as well as flexible working hours, private health care, life insurance and ongoing training and career development opportunities. You will be working for a respected Biopharmaceutical Services company.

ROLE DESCRIPTION

As a Clinical Project Director you will be responsible for the overall co-ordination and management of Phase II/III clinical trials, you will be directing the technical and the operational aspects of the projects and ensuring the successful completion of the trials. You will be working on a large scale global studies and will have oversight (but not line management) of several junior PMs but the core responsibility will still be hand-on Project Management.


REQUIREMENTS

*A Bachelor Degree in Life Science or related field
*Extensive Project Management experience within a CRO is a MUST for this role.
*Experience within Phase II/III global studies is desirable
*Good Negotiation techniques, and commercial and organizational acumen.
*Ability to lead, motivate and co-ordinate teams.


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.

www.i-pharmconsulting.com


TO APPLY

If you would like to discuss this vacancy further, please call Principal Consultant Natalie Hall on +44 (0)20 3189 0463, or email nhall@i-pharmconsulting.com. If this role is not suitable, Natalie is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


KEY WORDS:

Clinical Research Director / Clinical Project Director / PD / Project Manager / CPM / PM / Clinical Project Leader / Clinical Research / Clinical Research Scientist / Clinical Project Director / Director of Clinical Operations / Clinical Study Manager / Pharma / CRO / Senior CPM / Lead CPM / UK / England / Scotland / Wales / M4 / South-East / Middlesex / Berkshire / Surrey / London / The Netherlands /Europe / France / Belgium / Italy / Spain

I-Pharm Consulting Ltd


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