Company: i-Pharm Consulting
Reference: JS 14122016/NL
Closing Date: 24 Jan 17
Salary (£): Negotiable
Are you an experienced clinical Trials Assistant with + 3 years experience in clinical research?My client offers a brand new role in start-up for the right candidate to start ASAP!JOB TITLE Study startup specialistFulltimeFixed term contract of 12 months + possibility to go permanentOffice basedLOCATION NetherlandsNijmegen-ArnhemSALARY & BENEFITS Competitive salary -Reimbursement of Mileage -Pension – Healthcare- Life insurance – holiday payROLE/DESCRIPTION Manages the preparation, review an ...
Are you an experienced clinical Trials Assistant with + 3 years experience in clinical research?
My client offers a brand new role in start-up for the right candidate to start ASAP!
Study startup specialist
Fixed term contract of 12 months + possibility to go permanent
SALARY & BENEFITS
Competitive salary -Reimbursement of Mileage -Pension – Healthcare- Life insurance – holiday pay
Manages the preparation, review and coordination of Country Submissions in line with global submission
Ultimately responsible for study start-up in accordance with ICH-GCP guidelines.
Primary contact with investigative sites during site start-up activities.
Responsible for maintaining the study database during the whole clinical trial.
Attending investigator meetings, logistical support of clinical trial supply coordination
Involvement at feasibility stage.
Life Sciences Degree or equivalent, in a scientific or healthcare discipline
+ 3 years experience in clinical research
Strong working knowledge of the ICH guidelines and FDA, IRBIIEC regulations.
Experience in submissions!
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.
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