better Biotech Pharma Job in Kansas

Our client, a leader in healthcare information services, is looking for a Clinical Research Associate. This person will be responsible for all aspects of study initiation, including coordinating with various departments to ensure a smooth start-up. Additional responsibilities: - Presenting professional presentations at meetings - Monitoring sites and preparing reports for sponsor - Work with QA for study specifications - Review reports and release to sites - Traveling to investigator meetings This position will

Clinical Pharmacist Oncology, Transplant, HIV/AIDS - Overland Park, KS, Phoenix, AZ, Omaha, NE or St. Louis, MO (Relocation Offered) 216468 Job Description Submit Description Prescription Solutionshelps consumers obtain the medications and products they need to live healthier lives. Services offered by the company include pharmacy network contracting, rebate contracting and administration, mail order pharmacy facilities, specialty drugs and retail drug claims processing. The company is one of only three

Previous line management experience Profile Locations USA Kansas Overland Park Organization USA04 US CTS...

Profile Locations USA Kansas Overland Park Organization USA02 US Clinical Development Svcs...

Profile Locations USA Kansas Overland Park Organization USA02 US Clinical Development Svcs...

Profile Locations USA Kansas Overland Park Organization USA02 US Clinical Development Svcs...

Profile Locations USA Kansas Overland Park Organization USA02 US Clinical Development Svcs...

Clinical Research Associate CRA Sr CRA Kansas Missouri 0805978 Apply Online Description The Clinical...Profile Locations USA Kansas Overland Park Organization USA02 US Clinical Development Svcs...

Profile Locations USA Kansas Lenexa Organization USA02 US Clinical Development Svcs...

Director Biostatistics for our Overland Park Kansas office...in process improvement activities Profile Locations USA Kansas Overland Park Organization USA02 US Clinical Development...

Profile Locations USA Kansas Overland Park Organization USA02 US Clinical Development Svcs...

At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance s impressive history of company stability and growth. We ve achieved these results by fostering a work environment that encourages, develops and leverages our team s capabilities. Covance s ongoing success offers team members unsurpassed growth and career development opportunities. There is no better time to join us! The Medical

Job Classification: Direct Hire Description: Our client, a leader in healthcare information services, is looking for a Clinical Research Associate. This person will be responsible for all aspects of study initiation, including coordinating with various departments to ensure a smooth start-up. Additional responsibilities: - Presenting professional presentations at meetings - Monitoring sites and preparing reports for sponsor - Work with QA for study specifications - Review reports and release to sites -

Job Category:Pharmacy Operations Reference Code:216468 Position Type:Full-time Clinical Pharmacist Oncology, Transplant, HIV/AIDS - Overland Park, KS, Phoenix, AZ, Omaha, NE or St. Louis, MO (Relocation Offered) - 216468 Job Description Description Prescription Solutions helps consumers obtain the medications and products they need to live healthier lives. Services offered by the company include pharmacy network contracting, rebate contracting and administration

PRA International is a world leader in providing clinical research services to the pharmaceutical and biopharmaceutical industries. We serve some of the best-known companies in the world and work on many of the most advanced experimental drugs, Biologics and medical devices in development today. We currently have an excellent opportunities for a Clinical Project Manager and Clinical Project Directors. These positions can be office based at any of our US locations in NJ, PA, VA, KS, and CA or now can be regionally

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. Prescription Solutions helps consumers obtain the medications and products they need to live healthier lives. Services offered by the company include pharmacy network contracting, rebate contracting and administration,

our Specialty Pharmacy department in Overland Park Kansas...

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 Midwestern region. The clinical research

A career at Quintiles Transnational Corp. puts you at the corporate center of the leading worldwide pharmaceutical services organization. Quintiles is a $2B+ pharmaceutical services provider that is in the business of helping to speed life saving medicines to patients around the global. Currently we have nearly 20,000 employees worldwide that work and live in over 50 countries. If you want to work for a global, fast-paced organization dedicated to improving the development and marketing of medicines, Quintiles

A career at Quintiles Transnational Corp. puts you at the corporate center of the leading worldwide pharmaceutical services organization. Quintiles is a $2B+ pharmaceutical services provider that is in the business of helping to speed life saving medicines to patients around the global. Currently we have nearly 20,000 employees worldwide that work and live in over 50 countries. If you want to work for a global, fast-paced organization dedicated to improving the development and marketing of medicines, Quintiles

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

ClinForce is currently seeking a Regional Clinical Research Associates- CRAs for the Midwest, Northeast and West Coast. Successful candidate will be responsible for the following: - Prepare and conduct study initiation, close-out and monitoring visits at clinical investigative sites to ensure adherence to procedures, protocols and project plans in accordance with FDA regulations. - Maintain site files, trial master files and study documentation. - Develop status reports, SOP revisions and document quality control

Director Biostatistics for our Overland Park Kansas office...

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 Midwestern region. The clinical research

Clinical Pharmacology department in our Overland Park Kansas office is seeking an enthusiastic Clinical Data...

Qualifications - Bachelor s degree in clinical, biological or mathematical sciences, nursing degree or related field, with a minimum of 3 years experience in a clinical data management role, specifically in a CRO, pharmaceutical or biotech environment or the equivalent of education, training or experience. - Candidates must have prior work experience in a lead role, managing assigned projects on all levels, acting as the lead. - Candiate must have a thorough knowledge of the clinical trial data management

Clinical Pharmacology department in our Overland Park Kansas office is seeking a Clinical Data Manager...

Ophthalmology jobs in Overland Park, KS - - - - Send This Job to a Friend Search More Jobs CyberCoders - Be Selective Location Overland Park, KS; Lawrence, KS Salary $85

Responsibilities will include, but are not limited to, the following: Key Activities AE CASE MANAGEMENT Receipt Execute receipt of Drug Safety phone calls and complete telephone AE form Create phone call communication logs in ARISg Triage Support the triage of cases conducted by Sr Specialist as needed Assessment - Complex Case Support the assessment of complex cases conducted by Sr Specialist as needed Assessment - Non-Complex Case Execute QC on key fields of serious cases Create key fields

Clinical Pharmacology department in our Overland Park Kansas office is seeking a Clinical Data Manager...

Director Biostatistics for our Overland Park Kansas office...

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 - BS in life sciences or related field - 2+ years in Project Management environment - 5+ years of clinical research or related relevant experience - Experience in a key CRO/Pharmaceutical operational function, e.g., data management, clinical operations, laboratory, pre-clinical - Strongly prefer candidates with solid Phase II-IV management experience - Experience with resource and budget/financial management - Good written & oral communication skills - Good client management skills

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.

Qualifications - Bachelor s degree in clinical, biological or mathematical sciences, nursing degree or related field, with a minimum of 3 years experience in a clinical data management role, specifically in a CRO, pharmaceutical or biotech environment or the equivalent of education, training or experience. - Candidates must have prior work experience in a lead role, managing assigned projects on all levels, acting as the lead. - Candiate must have a thorough knowledge of the clinical trial data management