better Biotech Pharma Job in Missouri

includes more than 450 000 residents from Missouri Arkansas Oklahoma and Kansas...in Joplin the largest metropolitan area in Missouri Freeman Health System is a 404 bed...in clinical research or a current valid Missouri RN license required Certified Clinical Research Associate...

Site Location Kansas City Missouri Job Description Clinical Pharmacist Consultants function independently...

Manager of Clinical Development -Our client is one of the top Pharmaceutical Companies in the world. Due to their exponential growth in clinical trials, they are looking for a Manager of Clinical Development. The ideal candidate would have a DVM and MS with 5 years clinical experience. Manager of Clinical Development Requirements, 5 years experience with NDA s and other FDA regulatory compliance. Facilitates training for regulatory compliance. Directs and assigns development timelines. Develop and negotiate

The Kansas City Clinical Oncology Program (KCCOP) operating from the Brookside Campus of Research Medical Center has an immediate opening for a Clinical Research Associate (CRA). The CRA is an autonomously functioning person who coordinates various activities associated with cancer treatment studies available to the KCCOP. Achieves KCCOP's goals and objectives through data management, quality control, coordinative and liaison activities.. Job Requirements: I. Minimum Qualifications:A. Education:High School

Biostatistician Department: Internal Medicine/SLUCOR Recruiter: Cox Requisition Number: 11862 Date Posted: 02-07-2005 Status: FT Grade: 450 Min-Mid Salary: 3,883-5,047 JOB DESCRIPTION Job Summary: Under general direction, creates and maintains statistical databases; provides statistical assistance to faculty and staff; prepares scientific reports. CHARACTERISTIC JOB TASKS AND RESPONSIBILITIES May include any and/or all of the following: Provides statistical support and consultation to faculty for grant

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

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

City Hazelwwod State MO Job Title SR. BIOSTATISTICIAN Description The Senior SAS Programmer is responsible for designing, developing, validating, and maintaining both general purpose and ad hoc SAS programs used to support regulatory reporting from clinical trials. This role provides expertise in SAS programming and related programming processes to the Biostatistics group, and acts as lead programmer for one or more projects. Subject to the approval of the Director of Biostatistics, the Senior SAS Programmer

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

We're actively interviewing this month for a dynamic Regional Healthcare Provider. The hours are 11:30 - 9:00pm. No weekends. Great benefits, hours and plenty of room for advancement for the right person. We have all the upside of a large company and the flexibility of a Mom & Pop. Talk to us! You'll be glad you did. We'll contact you to answer your questions within 24 business hours. *Medical, Dental, Vision & Prescription Plans *Matching 401 K *Company Paid Life Insurance *Optional Life Insurance

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

Manager of Clinical Development -Our client is one of the top Pharmaceutical Companies in the world. Due to their exponential growth in clinical trials, they are looking for a Manager of Clinical Development. The ideal candidate would have a DVM and MS with 5 years clinical experience. Manager of Clinical Development Requirements, 5 years experience with NDA s and other FDA regulatory compliance. Facilitates training for regulatory compliance. Directs and assigns development timelines. Develop and negotiate

.SUMMARY OF POSITION: 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

City Hazelwood State MO Job Title Sr. Clinical Data Manager Description .SUMMARY OF POSITION: 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

Clinical Research Associate-Radiate Onc Department: Oncology Services Schedule: Per Diem Shift: Days Hours: 8-430 Job Details: Position Summary: Analyzes and evaluates clinical data. Gathers data and completes all protocol specific forms in a timely manner. Determines eligibility of patients for cancer treatment and prevention/control clinical trials. Maintains patient rights and confidentiality. Ensures compliance with protocols and overall clinical objectives. Communicates effectively with health care

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

Clinical Staff Pharmacist Jobs Missouri Job Location Northeast MO Category Pharmacy Clinical Pharmacist Apply Now... Back to Results Clinical Staff Pharmacist job in Northeast Missouri Hospital...Voted one of the top hospitals in Missouri...for this and other hospital jobs in Missouri...