better Biotech Pharma Job in Kansas

CLINICAL DATA COORDINATOR COMPANY INFO: As the world leader in workforce solutions, Adecco delivers an unparalleled range of career resources to our qualified associates. Our Adecco Technical office in Overland Park, KS offers clinical research opportunities in the pharmaceutical, and biotechnology industries. Our is client the world's largest CRO improving healthcare worldwide by providing a broad range of professional services, information, and partnering solutions to the pharmaceutical, biotechnology and

Clinical Data Coordinator Location: Overland Park, KS Category: Medical & Science Status: Temporary/Contract Reference: US_EN_2_105994_135213 Salary: N/A Posted: October 28,2009

PRA International is one of the world's leading global clinical research organizations, conducting clinical trials in 65 countries across six continents. PRA provides outsourced clinical services across all phases of pharmaceutical and biotech drug development. Through its 30+ years of experience, PRA has developed the operational and therapeutic expertise to provide high quality, global service while maintaining our differentiating PERSONAL ELEMENT of commitment to excellence. We currently have openings

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 a seeking enthusiastic Senior Biostatistician. The Senior Biostatistician will develop

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 a seeking enthusiastic Senior Biostatistician. The Senior Biostatistician will develop

CLINICAL DATA COORDINATOR COMPANY INFO: As the world leader in workforce solutions, Adecco delivers an unparalleled range of career resources to our qualified associates. Our Adecco Technical office in Overland Park, KS offers clinical research opportunities in the pharmaceutical, and biotechnology industries. Our is client the world's largest CRO improving healthcare worldwide by providing a broad range of professional services, information, and partnering solutions to the pharmaceutical, biotechnology

Staff/Clinical Pharmacist Kaye/Bassman International has been engaged by a 250 bed, suburban hospital to locate a Staff/Clinical Pharmacist for a new expansion position. This beautiful, financially sound Medical Center provides the surrounding communities with a number of medical specialties ranging from comprehensive cardiac and trauma care to family-based primary care services. The Director of Pharmacy is willing to train and mentor motivated pharmacists looking for more clinical exposure. Schedule:

a Clinical Data Coordinator in Overland Park Kansas...

Website: http://www2.kumc.edu/researchinstitute/ Job Title: Clinical Trials Project Manager Reports To: Regulatory Support Program Director, Clinical Research Development Office (CReDO) Job Description: Outlined below are the principal responsibilities associated with the position: This position will have responsibility for all research administration activities of assigned clinical trials for the Regulatory Support Program Division of the Clinical Research Development Office (CReDO

Member of clinical research team responsible for data management activities across multiple trials. Activities include assisting in data entry, query processing, site management, data reporting and other data management activities in support of clinical trial projects. ESSENTIAL FUNCTIONS: Perform data management activities on both paper based and Electronic data capture (EDC) studies. Major activities include: CRF data review, preparation for entry, query processing, discrepancy management

The research department at KCAA has been conducting clinical research trials for almost 2 years and boasts staff members with years of research experience. All of our physicians and providers are committed to research excellence. Topics of our trial expertise include seasonal and perennial allergies, asthma, allergic asthma, hereditary angioedema, chronic sinusitis, eczema, hives and allergy immunotherapy. Position Description: -Manages the conduct of clinical allergy and asthma investigations Position

Job Title Biostatistician Job Family Early Development Services PRA Location Lenexa, KS AutoReqId 7251BR JobDetails Prepares and performs statistical analysis on all relevant projects for clients and PRA staff. ACCOUNTABILITIES . Designs, develops, modifies, and evaluates the technical data and infrastructure to expedite and evaluate analysis and reporting of clinical and pre-clinical studies o Provides significant input into the preparation and review of clinical study protocols and consults in the development

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 Assistant Clinical Data Manager/Data Team Lead to join our team!

Job Descriptions: Responsibilities are based on business/project need and may include: On site monitoring (pre study, initiation, interm, and close-out visits); site management; report on monitoring visit activities/findings; communicate issues to in-house project team; possible co-monitoring; Investigator Meeting attendance/presentation. Travel will be 75-80%. Required Experience: BS/BA degree and a minimum of 2 years in monitoring clinical research studies are required. Must possess strong computer/telecommuting