Senior Clinical Research Associate - Home based

SENIOR CLINICAL RESEARCH ASSOCIATE | TOP 5 GLOBAL PHARMA | HOME BASED - NETHERLANDS

Senior CRA required for new positions with a global Pharma. If you are an experienced CRA and are looking for a new challenge we can offer a generous salary and package, flexible working arrangements (home or office based) with training and career development opportunities. This is a great position for any one that has been working as a Senior CRA that would be looking at a company where they can progress and take the next step in their career.

JOB TITLE

Senior Clinical Research Associate / Senior Clinical Research Monitor

LOCATION

Netherlands

BENEFITS

Generous Salary

Company car/Car allowance

Full Benefits Package

Industry leading training programmes with excellent ongoing career progression opportunities.

ROLE/DESCRIPTION

You will be involved in study start-up, site initiation, site monitoring and close out visits on assigned studies across multiple therapy areas. Your role will also include mentioring of a group of clinical staff that will include CTAs, CRAs. You will be working in a rapidly expanding part of the business with many opportunities for further career progression. National and international travel is an integral part of this role.

REQUIREMENTS

Life Sciences Degree or equivalent, in a scientific or healthcare discipline

3 years + monitoring experience

Experience working in a CRO or Pharma Company is desirable

Fluency in English and Dutch (preferable)

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 Mak Ishola on +32 (0)2 808 2151, or email mishola@i-pharmconsulting.com. If this role is not suitable, Mak is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEY WORDS

Clinical Site Monitor / Senior Clinical Site Monitor / CSM / Senior CSM / Sr CSM / CRA / CRA I / CRA II / SSU / Senior CRA / SCRA / Senior Clinical Research Associate / Lead CRA / LCRA / Monitoring /Monitor / Clinical Trial / Drug Trial / Trial Sites / Clinical / CRA 1 /CRA 2 / ICH-GCP / Clinical Research / Clinical Trials / Study Start-Up / Start-Up / Study Start Up / SSU / Clinical Study Start-Up/ Regulatory Affairs / Regulatory Documents / Regulatory Submissions / Ethical Submissions / ICH-GCP / GCPv / Central Europe / Eastern Europe / SCRA / Clinical / Home Based / Home-Based / Amsterdam / Rotterdam / Utrecht / Eindhoven / Den Haag / Nijmegen / Lent / Rotterdam / Arnhem / Breda / Maastricht / Tilburg /Groningen / Holland / Noord Holland /Zuid Holland / Noord Brabant / Nederland