better Biotech Pharma Job in Utah

Success through teamwork We work together to find a better way and break new ground to make progress possible. Focused on common goals, we raise the standard and make a difference. We strive for excellence in everything we do. At ICON, career possibilities can become realities for those who look for challenges and embrace learning and growth opportunities. ICON Clinical Research is dedicated to providing the pharmaceutical and biotechnology industries with exceptional clinical research and biometrics services

Success through teamwork We work together to find a better way and break new ground to make progress possible. Focused on common goals, we raise the standard and make a difference. We strive for excellence in everything we do. At ICON, career possibilities can become realities for those who look for challenges and embrace learning and growth opportunities. ICON Clinical Research is dedicated to providing the pharmaceutical and biotechnology industries with exceptional clinical research and biometrics services

Job Title Mgr, Clinical Research AutoReqId 6202BR Job Description Under general direction, plans, coordinates and executes function specific clinical research programs for the clinical evaluation of products. Supervises assigned department staff. Essential Job Functions: . Serve as Team Lead for the execution of assigned projects which includes, but is not limited to; resource allocation, timelines, quality of deliverables, and budget management. Communicate project timelines and priorities to all the multidisciplinary

Clinical Research Associate CRA Sr CRA Utah 0805912 Apply Online Description The Clinical Development...Profile Locations USA Utah Salt Lake City Organization USA02 US Clinical Development Svcs...

Kendle, a leading clinical research organization, is seeking experienced Clinical Research Associates (CRAs) with one to four years of regional site monitoring experience. Kendle offers a travel expectation of 60 - 80% averaging up to three overnight stays per week, career advancement that can be home-based up to and including Project Leader (Project Manager) as well as a company core value to have a balance between work and life. Key Responsibilities CRAs at Kendle complete project activities associated

Description 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 Western region. The clinical

At University of Utah Health Care we are relied on by...a Clinical Pharmacist with the University of Utah Hospital Pharmacy you have the opportunity to...Check us out online at www jobs utah edu and fill out an online application...The University of Utah is an Equal Opportunity Affirmative Action employer...

life insurance benefits to active and retired Utah public employees and their beneficiaries...About The Company Utah Retirement Systems provides financially sound retirement and...Currently licensed to practice pharmacy in the state of Utah required with a clean licensing history record without infractions...

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 Western region. The clinical research

Position Description Position Title: Clinical Research Coordinator Reports To: Associate Director Clinical Operations Position Purpose/Summary Responsible for coordinating and conducting research protocols in a manner that ensures quality, consistency, timeliness, accuracy and patient safety. Frequent face-to-face, written, and telephone contacts with various persons involved in the study including but not limited to the patients, relatives/friends of the patients, doctors,

Position Title: Clinical Assistant I Reports To: Supervisor of Clinical Operations Position Purpose/Summary Assists clinical staff in conducting research protocols, with occasional face-to-face and telephone contact with various people involved in the study. Essential Job Functions - Assists in conducting research protocols in a manner that ensures quality, consistency, timelines, accuracy and patient safety - Conducts screening visits with potential study patients

Utah Licensure eligible...

About Medpace: Medpace is a global, full-service contract research organization (CRO), headquartered in Cincinnati, OH, that provides comprehensive clinical research support to the pharmaceutical industry. In over 15 years of existence, we have grown to become a global company with operations in almost 40 countries and now have the reach to conduct clinical trials worldwide. While continuing to maintain a strong presence in Cincinnati, Medpace was named one of the fastest growing private companies in North

Job Description Submit Description i3 Research is a full-service contract research organization (CRO) focused on four CORE areas: central nervous system; oncology; respiratory and infectious disease; and, endocrinology and metabolic disease. Therapeutic specialization drives all aspects of business in this global CRO from project staffing and talent management to quality initiatives, such as six sigma. As a UnitedHealth Group company, i3 Research is part of a worldwide health care

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.

Job Description JOB DESCRIPTION: Experienced Clinical Research Associate # 293251 Success through teamwork We work together to find a better way and break new ground to make progress possible. Focused on common goals, we raise the standard and make a difference. We strive for excellence in everything we do. At ICON, career possibilities can become realities for those who look for challenges and embrace learning and growth opportunities. ICON Clinical Research is dedicated to providing