Ref #: 26968

Employment type: Permanent - Full-Time

Location: US - West Coast

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.
The role

Working independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation

Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested

Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required

Managing sponsor generated queries efficiently and responsible for study cost effectiveness

Dependent on level of experience you may assist in training and mentoring less experienced CRA's and/or manage CRA's working on international projects

What you need:

Minimum of 1 year of active independent field monitoring experience- all types of visits.

Bachelor's degree required.

Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data

Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner

Ability to produce accurate work to tight deadlines within a pressurized environment

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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