Ref #: 27476

Employment type: Permanent - Full-Time

Location: Northeast US

Description

Why join the DOCS team at ICON?

Working at ICON is more than a job, it’s a calling for people who care and are passionate about improving patients’ lives. At ICON, we care about our people and your passion, you are key to our success. We aim to provide an open and friendly work environment where we empower our people and provide them with opportunities to develop their long-term career.

•A Clinical Research Associate is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from study planning through data-base lock.
•Responsibilities include study planning, study start-up, study execution and study close-out.
•Delivers results that have direct impact on the successful completion of the study.
•Partner with the Clinical Trial Associates and Clinical Study Managers to ensure overall site management while performing study related activities for assigned protocols.

Qualifications:
•Bachelor’s degree required
•Must have experience in Clinical Research
•A Minimum 1 year of monitoring experience

Travel: up to 70% travel

DOCS is the FSP division of ICON Clinical Research. We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.

DOCS is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.

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