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Global clinical trials specialist

Melbourne
beBeeClinicalResearch
Posted: 5 October
Offer description

Job Opportunity

Clinical Research Associate II & Clinical Research Associate III, Senior Clinical Research Associate sought after for global clinical trials across phases I-III in various therapeutic areas.

About the Role:

* Independently conduct site visits including site selection, initiation, monitoring, close out and database lock.
* Ensure correct clinical documentation such as CRF to maintain sites compliance with industry guidelines.

Key Responsibilities

1. Conduct global clinical trials across phases I-III, therapeutic areas including oncology, cardiovascular, neurology etc.
2. Site selection and initiation, monitoring, closeout and database lock.
3. Ensure correct clinical documentation.

Requirements

* At least 12 months experience working as a Clinical Research Associate (CRA) in pharmaceutical/life science industry conducting independent monitoring visits.
* Degree educated in related scientific field.
* Experienced independent monitoring.

Benefits

* Company prioritizes career development and has strong supportive culture.
* Join company with 20 years of proven success achieving consistent growth over past five years.

Other Information

* This role is suitable for someone with at least 6 months independent monitoring experience in CRO or Pharmaceutical company.
* Company will conduct interviews soon.

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