better Biotech Pharma Job in Kentucky

***Regional Clinical Research Associate for i3 Research- Midwest (Contract or Perm) 214180 Job Description Submit Description i3 Research is a full-service, global CRO specializing in centralnervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. We approach our work with an intense focus on the unique demands of these therapeutic categories and the needs of our clients. We deliver the therapeutic science that helps our clients develop better

Profile Locations USA Kentucky Lexington Organization USA02 US Clinical Development Svcs...

Clinical Research Associate / CRA / Senior CRA / Lexington 0806008 Job Description of Clinical Research Associate / CRA / Senior CRA / Lexington 0806008 The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves

Description i3 Research is a full-service, global CRO specializing in central nervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. We approach our work with an intense focus on the unique demands of these therapeutic categories and the needs of our clients. We deliver the therapeutic science that helps our clients develop better patient care. As a UnitedHealth Group company, i3 Research is part of a worldwide health care service organization that

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health. i3 Research is a full-service, global CRO specializing in central nervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. We approach our work with an intense

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health. i3 Research is a full-service, global CRO specializing in central nervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. We approach our work with an intense

The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic CRA to join the team in our Southeast region. The clinical research

Qualifications Qualifcations: - B.A./B.S. Degree in related field, or an equivalent combination of education and work experience - Five + years relevant clinical data management experience - Previous management experience or demonstrated leadership ability - Ability to work in and lead multi-disciplinary/cultural teams - Proven ability to effectively recruit and develop staff - Proficient in the use of the clinical data management systems used at i3 Statprobe - Ability to prioritize

Qualifications Qualifications: - MS degree required with a minimum of five years experience in statistics or PhD with two years of experience in statistics - Ability to work in a fast-paced, team-oriented environment - Computer proficiency is required - Ability to perform statistical analyses of clinical data - Ability to define problems, collect data, establish facts, and draw valid conclusions - Ability to interpret an extensive variety of technical instructions in mathematical or

Qualifications - Prefer BS/BA. - 1 year monitoring experience or combination of on-site monitoring and clinical research coordinator experience. - Customer service orientation. - Sound knowledge of medical terminology and clinical monitoring process. - In depth therapeutic and protocol knowledge as provided in company training. - Ability to perform regionalized travel an average of 65%, depending on project needs. - Excellent verbal and written communications skills.