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Job Details

Clinical Study Monitor /Clinical Trials Administrator – NL

Company: Amoria Bond
Location: Netherlands
Reference: J59204
Closing Date: 14 Dec 16
Type: Contract
Salary (£): Negotiable
Benefits:

Job Summary:

Clinical Study Monitor /Clinical Trials Administrator – NLA large, global pharmaceutical company is looking for a Clinical Study Monitor/Clinical Trials Administrator in The Netherlands. The role combines monitoring tasks with project administration duties. A great opportunity for someone with a various skill set and track record in CRA/study specialist functions. The function offers the opportunity to work home based for 1 or 2 days per week. ...

Requirements:

Clinical Study Monitor /Clinical Trials Administrator – NL

A large, global pharmaceutical company is looking for a Clinical Study Monitor/Clinical Trials Administrator in The Netherlands. The role combines monitoring tasks with project administration duties. A great opportunity for someone with a various skill set and track record in CRA/study specialist functions.

The function offers the opportunity to work home based for 1 or 2 days per week. The duration is around 6-12 months and the location is in the south of Holland.

The successful candidate will work across a series of clinical studies and projects mainly in the start-up phases and will be responsible for but not to be limited to:
- CRA tasks and monitoring of studies
- Assists project managers in the production of study reports and updates.
- To review and negotiate all regulatory documents for completeness
- Provides administrative support to the project teams in clinical operations in accordance with ICH GCP, Orion SOPs and local regulations.
- Able to identify activities along the critical pathway towards the start-up and completion for a study

Skills & Experiences
• Degree in life sciences or equivalent work experience
• Knowledge of ICH GCP/FDA regulations
• Excellent team player, collaborative and able to enable an effective team
• Excellent organisational and time-management skills, able to meet deadlines
• Self-starter with lots of common sense and able to act on own initiative

Are you the person with the various skill set we’re looking for? Then apply now!

CRA, Worksheet reviews, Set up, trial master files, in-house monitoring, coordination, administration, quality, analysis, communication, newsletters, reports, reviews, documentation, research, project management, coordination, administration, submissions, compliance, support

Amoria Bond operates as an employment agency and employment business. No terminology in this advert is intended to discriminate on the grounds of age or experience, and we confirm that we are happy to accept applications from persons of any age or experience for this role.

Apply for this job: Clinical Study Monitor /Clinical Trials Administrator – NL

Contact Information:

Address:  Head Office
Keizersgracht 270, 1016 EV Amsterdam, Nederland.

Netherlands
Tel:  +31 (0) 20 80 80 888
Website:  Visit Our Web Site

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