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Project Manager - Study Start Up - UK

England£0.00 per annum

Clinical Project Manager - Study Start Up & Regulatory (UK/home based)

A Clinical Project Manager is required by an industry leading CRO to join their study start up and Regulatory team. Your role will be to manage and over execution of the start up of sites in one or multiple Phase II through Phase IV clinical trials across all functional Site Start-Up areas.

Clinical Project Manager /Senior Project Manager / Senior Clinical Project Leader / Study Start Up.

UK / England / Scotland / Wales/ France/ Germany/ Netherlands / M4 / South-East / Middlesex / Berkshire / Surrey / London / Belgium / Italy / Spain


Competitive Salary
Car Allowance & Bonus
Flexible working hours
Private Health Care
Life Insurance
Ongoing Training and Career Development Opportunities


As a Clinical Project Manager in Study Start Up you will be expected to undertake full lifecycle and cross functional responsibilities which will include:

*Provides oversight of all the project study start up activities: site selection to site activation-ready.
*Responsibility for study start up deliverables at the project level following the project requirements and the applicable plans.
*Act as the primary global liaison during Study start up
*Assisting in the management of multifunctional leads associated with Study start up.
*Site selection, site set up, clinical trial regulatory works such as reg submissions, communication to the relevant authorities/ethics committees import licences, study maintenance submissions.
*Essential document collection leading to site activation, Site contract management; and overall timeline management


*A Life Science or Nursing Degree
*Experience in clinical research, including previous CRA and Project Management Experience, study start up experience is also ideal.
*Experience in CRO sector is desirable
*Strong communication and interpersonal skills, including good command of English language
*In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and ICH guidelines


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 Natalie Hall on +44 (0)20 3189 0463, or email 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.


Clinical Project Manager / Project Manager / CNS / CPM / PM / Clinical Project Leader / Clinical Research Associate / CRA / Clinical Research / Clinical Research Scientist / Project Manager / 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// Belgium / Italy / Spain

March 06, 2013
April 05, 2013
Natalie Hall
Clinical Practice
Full Time