Clinical Research Associate (US)
ICON Clinical Research - United States

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Clinical Research Associate (US) - 003332

                          Clinical Research Associate with ICON at ACRP

                          Come visit us at the ACRP in Orlando, FL

                          This is an exciting opportunity to work within a fast paced, busy environment at ICON , a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.

                          We welcome you to visit us at the ACRP Conference in Orlando, FL April 13-16 at Booth 435.

                          Meet a member of our team to discuss CRA Opportunities.

                          At ICON, it's our people that set us apart:
                          • $5000 Sign-ON Bonus
                          • $3000 Internal Referral Bonus
                          • Health, Medical, Dental, Vision, STD, LTD Coverage
                          • 401k - Fully vested from hire date
                          • Tuition Reimbursement
                          • Flexible Spending Account
                          • Compressed work week schedule
                          Overview of the Role:
                          • Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.
                          • Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required
                          • Approximately 65-75% travel overall can be expected, regional and national.
                          • In line with our philosophy of providing the highest quality to our clients, CRAs are typically assigned to one to two programs at a time.
                          Role Requirements / Skills / Experience:
                          • Applicant should possess a B.S. degree in life science, nursing or an equivalent combination of education and work experience (RN or LPN with at least 4 year of field monitoring experience).
                          • Applicants must have at least 3 years of experience independently monitoring clinical trials.
                          • Knowledge of ICG GCP guidelines and the expertise to review and evaluate medical data.
                          • Ability to travel overnight, primarily in the U.S., 3+ days per week on average.
                          ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment

                          Job : Clinical Research Associate
                          Primary Location : US

                          Organization : Clinical - CRA Management

                          Job Posting : 21/Mar/13, 6:53:22 PM

                          ICON Clinical Research - 23 months ago - save job
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                          Contract research organization (CRO) ICON is not iconic yet, but it would like to be. By the time a new drug hits the market, it has passed...