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Job Details

Study Management Associate

Company: i-Pharm Consulting
Location: West London
Reference: DWILL23
Closing Date: 23 Nov 17
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

JOB SUMMARY • Study Management Associate• Elite Biotech with strong varied pipeline • Historical gateway into Global Study Management and Senior Management • Outstanding working environment and professional support • Excellent remunerationLOCATION • West LondonRESPONSIBILITIES • Program management for assigned projects • Pre-clinical and clinical document coordination in line with FDA/EMA requirements • Budget management for assigned projects • Vendor management for all outsourced trials • A ...

Requirements:

JOB SUMMARY
• Study Management Associate
• Elite Biotech with strong varied pipeline
• Historical gateway into Global Study Management and Senior Management
• Outstanding working environment and professional support
• Excellent remuneration

LOCATION
• West London

RESPONSIBILITIES
• Program management for assigned projects
• Pre-clinical and clinical document coordination in line with FDA/EMA requirements
• Budget management for assigned projects
• Vendor management for all outsourced trials
• Applying research regulatory requirements, GCP and ICH
• Liaising with internal and external stakeholders for investigator meetings and documentation, CTA submissions and protocols

REQUIREMENTS
• Bachelor of Science or Bachelor of Nursing Degree
• Proven clinical monitoring background
• Strong Oncology experience
• Competent in written and oral English
• Excellent organisational skills
• Eligible to work in the UK
• Full UK drivers licence

BENEFITS
• Private healthcare
• 25 days’ annual leave
• Pension
• Life assurance
• 10% annual bonus


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 learn more about this opportunity, please call Senior Consultant Dominic Williams on +44 (0)20 3873 7066, or email dwilliams@i-pharmconsulting.com. If this role is not suitable, Dominic is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEY WORDS

Clinical Trial Manager / Trial Manager / Project Manager / Clinical Project Manager / Clinical Trial Management Associate / Clinical Project Management Associate / Lead CRA / Principal CRA / CNS / Rare Disease / Rare Disease / East London / West London / South London / North London / Hertfordshire / Slough / Uxbridge / Maidenhead / London / Office based / Monitoring / Trials / Studies / Protocols / SCRA / LCRA / MHRA / Study Start Up / Clinical Research Associate / Clinical Monitor / Senior CRA / South East England

Apply for this job: Study Management Associate

Contact Information:

Address:  Head Office
212 New King’s Road London
SW6 4NZ
England
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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