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Site Monitor/ Clinical Research Associate

Company: ICON plc
Location: Idanha
Posted on: January 13, 2022

Job Description:

The Clinical Research Associate is ultimately responsible for the successful management of investigator sites and monitoring activities for assigned clinical studies throughout the trial lifecycle.

Requirements:
Education: Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required

Skills:
5+ years of clinical independent monitoring experience required
Read, write and speak fluent English; fluent in host country language required.
Knowledge of ICH and local regulatory authority regulations regarding drug
Clinical research experience
Knowledge of ICH and local regulatory authority regulations regarding drug
An advanced degree (e.g., M.S., M.B.A., PharmD, etc)
Experience in monitoring all trial components (PSSV to COV)
Experience in coaching/mentoring other CRAs

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

Keywords: ICON plc, Salem , Site Monitor/ Clinical Research Associate, Healthcare , Idanha, Oregon

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