Company: i-Pharm Consulting
Closing Date: 27 Mar 17
Salary (£): Negotiable
Clinical Research Associate II - Senior Clinical Research Associate - MelbourneGlobal CRO, to be part of their core team or outsourced to a remarkable Pharmaceutical organisation.
Clinical Research Associate II – Senior Clinical Research Associate – Melbourne
Global CRO, to be part of their core team or outsourced to a remarkable Pharmaceutical organisation.
What does a CRA Do?
A clinical research associate (CRA) runs clinical trials to test drugs for their effectiveness, risks and benefits to ensure that they are safe to allow on to the market. You may work on new, as well as existing drugs and will usually be employed by either a pharmaceutical company or a contract research organisation (CRO), which works on behalf of pharmaceutical companies.
My clients offer a range of flexibility whether it is working from home, reduced travel or .8FTE as well as a great salary, car allowance and other flexible benefits.
•Help organise and monitor different phases of the clinical trials
•Writing drug trial methodologies
•Identifying and briefing appropriate trial investigators
•Monitoring the progress throughout the trial
•Collecting all the data forms
•Performing site initiation, routine monitoring and close-out visits of sites
•Participating in site start up, feasibility and/or site identification activities
•Assisting with the day-to-day management of clinical trials
•A must is: At least 6 months Local (Australian) independent monitoring experience
•Ability to work independently and demonstrate self – Management
•Experience with working across multiple studies and sites
•Excellent communication skills – verbal and written
•Commercial awareness, ICH-GCP Guidelines
About i-Pharm Consulting:
i-Pharm Consulting is a specialist Recruitment Company servicing the global Pharmaceutical industry. 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 Recruitment Consultant Jo Aitken on +61 (0) 2 8310 5842, or email firstname.lastname@example.org. If this role is not suitable, Jo is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
Permanent / Clinical Research / CRA I / CRA / Clinical Research Associate / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits / CRO / Global CRO // Pharma / Global Pharma Companies / Home-based / Clinical Monitoring / Sydney /Australia/ Nationwide Travel
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