Job description

Requirements

  • Entry level
  • No Education
  • Salary £80,000.00 - £99,999.00 gross per year
  • BELGIUM BE

Description

Study Start Up Specialist - 3-month contract - Global CRO - 1.0 FTE


i-Pharm Consulting are seeking on behalf of a Global mid-sized CRO a freelance Study Start-Up Specialist. Our client is a leader in clinical research and development and has strong relationships with a large number of global pharmaceutical companies.


THE ROLE:
Initial 3 month contract with the potential to extend. To manage the coordination of country submissions and clinical study start up activities in the Netherlands or Belgium. The ideal candidate is already a contractor and can start within 1 month.


Other duties include:


- Responsible for clinical trial set up including;
- End-to-end site start-up pre-award feasibility
- Coordinate country submissions
- Ethics Submissions
- Regulatory Submissions
- Support coordination of feasibility
- Negotiate site budgets


LOCATION:
Home Based - the Netherlands or Belgium

CONTRACT:

3 month contract - possibility of getting extended


RATE:
Competitive Hourly Rate


REQUIRED:


- Life sciences degree
- 3+ years within Pharmaceutical/CRO industry
- Strong SSU/CRA/Regulatory background
- Experience managing ethics and regulatory submissions in the UK and/or Ireland is essential
- Good knowledge of clinical research processes including ICH GCP


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 Youssef Maachou on +31 20 808 14 84, or email ymaachou@i-pharmconsulting.com. If this role is not suitable, Youssef is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


KEYWORDS:
SSU / Study Start Up / Start Up / Ethics / Regulatory / Country Approval Specialist / CAS / Submissions / Freelance / Contract / CRO / Clinical Research / Clinical Research Organisation / Pharma / i-Pharm / Home Based / Nederland / the Netherlands / België / Belgium / Amsterdam / Brussel / Rotterdam / Antwerpen / Den Haag /

  • scientists and researchers