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Job Details

CRAs Taiwan, Australia and South Korea/Clinical Research Associate

Company: Chiltern
Location: Asia Pacific - Australasia
Reference: MLJAPAC
Closing Date: 16 Dec 18
Type: Full Time
Salary (£): On Application
Benefits: NEGOTIABLE per country.

Job Summary:

We are actively looking for experienced CRAs who would be looking to be based in Taiwan or South Korea or Australia and who are legally authorized to work in these countries. Our focus at the moment is on "expats" who may be based in the EMEA region but are looking to relocate back home to the APAC region OR you may be based out in Taiwan, South Korea or Australia already and are actively seeking a new monitoring role.

Requirements:

We are actively looking for experienced CRAs who would be looking to be based in Taiwan or South Korea or Australia and who have the elligibility to live and work in these countries.

Our focus at the moment is on "expats" who may be based in the EMEA region but are looking to relocate back home to the APAC region OR you may be based out in Taiwan, South Korea or Australia already and are actively seeking a new monitoring role.

For these roles you would be employed permanently by Covance and outsourced to a Sponsor - dedicated 100% of the time to one Client, working to their SOPs and working along side their project teams. This is a home based position.

You will be working within our Flexible Solutions department dedicated to one sponsor/client.

Responsibilities include:

Full and idependent site management.

Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks

Negotiation of study budgets with potential investigators

Serious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs.

Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems

Education / Qualification

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)

Experience

Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines

Excellent understanding of Serious Adverse Event (SAE) reporting

Ability to resolve project-related problems and prioritize workload for self and team

You have previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)

If this is something you may be interested in can you please contact Marc Joseph on 0044 1753 216664 or email your CV to marc.joseph@chiltern.com at your earliest convenience.

key words monitoring, Asia Pacific, APAC, EMEA, CRA, clinical research associate, senior CRA, senior clinical research associate, site management, clinical monitor, Australia, South Korea

 

Apply for this job: CRAs Taiwan, Australia and South Korea/Clinical Research Associate

Contact Information:

Address:  London, UK
Covance Clinical and Periapproval Services Ltd Osprey House Maidenhead Office Park Westacott Way Maidenhead
SL6 3QH
England
Tel:  +44 (0) 1753 512000
Fax:  +44 (0) 1753 511116
Website:  Visit Our Web Site

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