Company: i-Pharm Consulting
Reference: JS - 7565-NL
Closing Date: 02 Mar 17
Salary (£): Negotiable
*Nominated one of the most admired CROs* (2015)CRA II, sCRANetherlandsBe more involved at the CRO4-8 visits/ monthCareer progression Ongoing studies and opportunities to enlarge your knowledge in therapeutic areas.Flexible workingCompetitive salary!Call me +44 203 005 79 45 or e-mail me jshikayi@i-pharmconsulting. ...
*Nominated one of the most admired CROs* (2015)
CRA II, sCRA
Be more involved at the CRO
4-8 visits/ month
Ongoing studies and opportunities to enlarge your knowledge in therapeutic areas.
Call me +44 203 005 79 45
or e-mail me email@example.com
Conversations and exchanged informations are treated with the greatest discretion!
SALARY & BENEFITS
Competitive salary / Car or Car allowance /Pension /Healthcare / Life insurance / Meal vouchers / Holiday pay
Working with a study team and/or for a sponsor
Ultimately responsible for managing the investigator sites in accordance with ICH-GCP guidelines
Involvement at feasibility stage, with responsibility for the site right through to close-out.
Operating as a key part of a global study team, the CRA plays a fundamental role in the sponsors drug development process.
Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, challenging projects.
Life Sciences Degree or equivalent, in a scientific or healthcare discipline
Min. 3 years experience ( initiation, monitoring and close-out visits)
Full understanding of the Serious Adverse Event (SAE)
Experience working in a CRO
Good communication, planning, organization and problem solving skills.
Fluency in Dutch and English
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.
If you would like to discuss this vacancy further, please call Principal Consultant Josette Shikayi on +44 (0)20 3005 7945, or email firstname.lastname@example.org. If this role is not suitable, Josette is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
CRA / CRA II / Senior CRA / SCRA / Senior Clinical Research Associate / Lead CRA / LCRA / Monitoring /Monitor / Clinical Trial / Drug Trial / Trial Sites / Clinical/CRA 2 / ICH-GCP / Clinical Research /Central Europe /AAmsterdam/ Haarlem/ Utrecht /Rotterda /Nederland
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