IQVIA Clinical Research Associate (GFR-B) in Missouri


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.


You should have:

  • A Bachelor's degree in a health care or other scientific discipline or educational equivalent

  • At least 6 months of on-site monitoring experience

  • Experience in Cardiology a plus

  • 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 a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.

Job Field:

Clinical Research & Monitoring

Primary Location:

United States

Other Location(s):

USA-Alaska, USA-New Hampshire, USA-Montana, USA-Rhode Island, USA-Utah, USA-Maine, USA-Maryland, USA-Oklahoma, USA-Arizona, USA-Wisconsin, USA-Minnesota, USA-North Dakota, USA-Kentucky, USA-Nebraska, USA-Connecticut, USA-Kansas, USA-Delaware, USA-Oregon, USA-New Jersey, USA-Wyoming, USA-Iowa, USA-Colorado, USA-Missouri, USA-Illinois, USA-Ohio, USA-Nevada, USA-Tennessee, USA-Pennsylvania, USA-Arkansas, USA-Mississippi, USA-Indiana, USA-Hawaii, USA-California, USA-Georgia, USA-Vermont, USA-Texas, USA-Michigan, USA-Virginia, USA-New York, USA-New Mexico, USA-West Virginia, USA-North Carolina, USA-Massachusetts, USA-South Carolina, USA-Alabama, USA-Idaho, USA-Florida, USA-Louisiana, USA-Washington, USA-South Dakota

EEO Minorities/Females/Protected Veterans/Disabled