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Clinical research associate (cra)

i-Pharm Consulting
Clinical Research Associate
Posted: 25 March
Offer description

Clinical Research Associate II | Australia | FSP & FS Available

Working either 100% sponsor dedicated or across multiple sponsors. Multiple positions have become available to join a fast growing, mid-size, CRO. This company are leaders in the industry and have a huge portfolio spanning across oncology, respiratory, cardiovascular, neurology and many more.

There are multiple opportunities available to suit a Clinical Research Associate (CRA) II - from 18 months independent monitoring.

You will be responsible for conducting 6-8 site visits per month and so offer a good work life balance.

Key Responsibilities:

* Working on global clinical trials across phases I-III, across oncology, cardiovascular, neurology and other therapeutic areas.
* Independently conduct regular site visits, this includes site selection, initiation, monitoring, through to close out and database lock.
* Responsible for ensuring correct clinical documentation, such as CRF, to ensure sites are compliant in line with relevant industry guidelines.

Confirmed Title and Salary:

* Title: CRA, Clinical Research Associate - I, II, III/Senior

This company will be conducting interviews in the coming weeks and so do not hesitate to apply if you are interested. Please send your CV to Keeley Munday at kmunday@i-pharmconsulting.com, call on 0426933037, or apply direct to this link for a further confidential discussion.

Desired Skills and Experience

Required Skillset:

* At least 18 months experience working in the pharmaceutical/life science industry as a CRA
* Degree educated in a related scientific field.

Associated Keywords: CRA, Clinical, Pharmaceutical, Pharma, CRO, Clinical Research Organisation, Clinical Research Associate, Australia, Melbourne, Sydney, Adelaide, Western Australia, WA, Southern Australia, SA, Northern Territory, Oncology, Respiratory, Cardiovascular, Monitoring, Sites, SIV, Database Lock.

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