Clinical Research Associate (GFR-L) Regional Travel

QuintilesIMS - United States3.9

Full-time
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As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA™ , we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits.

While projects vary, your typical responsibilities might include:

Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Supporting the development of a subject recruitment plan
Establishing regular lines of communication plus administering protocol and related study training to assigned sites
Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.
Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.
Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Project Manager (CPM), Clinical Research Specialist (CRS) and/or line manager.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Act as a mentor for new clinical staff.
May provide assistance to the Clinical Project Manager and/or CRS with design of study tools, documents and processes.
Qualifications

You should have:
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
At least 12 months of on-site monitoring experience
Experience in any complex therapeutic area
Alternatively, you should have an equivalent combination of education, training and experience

If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team.

IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.

“Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest conviction records”

Did You Know?

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.Whatever your career goals, we are here to ensure you get there!We invite you to join IQVIA™.

Primary Location: United States
Other Locations: USA-Illinois-Carbondale, USA-California-Anaheim, USA-Illinois-Bloomington, USA-Arizona-Phoenix, USA-New Hampshire, USA-New York-New York City, USA-North Carolina-Raleigh, USA-North Carolina-Durham, USA-Maine, USA-Maryland, USA-North Carolina-Charlotte, USA-Oklahoma, USA-Arizona, USA-Wisconsin, USA-Minnesota, USA-Kentucky, USA-Connecticut, USA-Kansas, USA-Illinois-Chicago, USA-Delaware, USA-Oregon, USA-New Jersey, USA-Colorado, USA-Missouri, USA-Illinois, USA-Ohio, USA-Nevada, USA-Massachusetts-Boston, USA-Tennessee, USA-Pennsylvania, USA-Mississippi, USA-Indiana, USA-California, USA-California-San Diego, USA-Georgia, USA-Vermont, USA-Texas, USA-Michigan, USA-California-Los Angeles, USA-Virginia, USA-New York, USA-California-Irvine, USA-New Mexico, USA-North Carolina, USA-Massachusetts, USA-Florida, USA-Louisiana-New Orleans, USA-California-San Jose, USA-Washington
Organization: USA02 - US Clinical Development Svcs
Job: Clinical Research & Monitoring