This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message
NextPharmaJob.com for pharmaceutical industry jobs
i-Pharm Consulting
NextPharmaJob.com is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Clinical Research Associate (CRA)
Italy
Clinical Research Associate (CRA)
Italy
Scientist/Senior Scientist
USA - Massachusetts
Senior Clinical Research Associate (Senior CRA)
Italy
Clinical Research Associate (CRA)
Italy
More...

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister sites:
Our sister site Our sister site
Partner sites:

At Burntsky Limited we work with a number of third parties in order to maximise the reach of the jobs posted with us including but not limited to:

JooblePartner Jooble
UK Jobs
Science Jobs

Job Details
This job has expired. Click here to view similar jobs.

CRA II/ SCRA - Regional Monitoring - One Site



Business Type: Clinical Research Organisation
Job Type: Clinical Research Associate (CRA), Senior Clinical Research Associate (SCRA)
Job Level: Management
Position: Full Time
Location: United Kingdom
Reference: CNOB780
Closing Date: 30/01/20
Job Details:

i-Pharm consulting is seeking an experienced CRA to work alongside a small CRO with an international presence. This position is an immediate requirement. This company strives to ensure a strong work-life balance for their employees and thus proves to be a sound opportunity for a motivated CRA. You will be outsourced to a top Pharma company and work across early phase Oncology studies. You will have one site in Nottingham.

LOCATION

UK - Ability to travel to one site in Nottingham

RESPONSIBILITIES

  • Working directly with the sponsor you will implement and monitor trials across a broad spectrum of therapeutic areas including Oncology
  • Applying research regulatory requirements, GCP and ICH
  • Present trial protocols at investigator meetings
  • Liaise between study site personnel and the company

REQUIREMENTS

  • Bachelor of Science or Bachelor of Nursing Degree
  • 2+ years monitoring experience
  • Competent in written and oral English
  • Entitlement to work in Ireland
  • Full drivers licence

BENEFITS

  • Excellent Salary
  • Car allowance
  • Healthcare
  • 25 days'' annual leave
  • Pension

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 Business Manager Ciara Noble on +44 (0)20 31890469, or email cnoble@i-pharmconsulting.com. If this role is not suitable, Ciara is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEY WORDS

CRA / Clinical Research Associate / CRA II / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / Oncology / Cardiovascular / Ophthalmology / Rheumatology / Republic of Ireland / Leinster / Dublin / Northern Ireland /Belfast / Cork / Galway / Donegal / Mayo / Contract Research Organisation / Pharmaceutical / Sponsor / Field Based / Office Based/ Global Pharma / Single Sponsor / Pharma Industry / Routine Monitoring / Site Initiation Visits / Close Out Visits /



Posted: 23/01/2020 | NPJ Ref: 249102
line graphic

Compatible with:

JobMate   Broadbean   Idibu

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing




Credit cards image