If you thrive in a fast-paced environment, are passionate about excellence, skilled at multi-tasking, and are detail oriented we would like to speak with you about joining our team! We are looking for candidates who demonstrate professionalism and are interested in building relationships, challenging themselves to meet established goals, and providing a quality work product. Job Summary: Responsible for collecting and transmitting data gathered from designated retail stores primarily using a hand-held scanning
If you thrive in a fast-paced environment, are passionate about excellence, skilled at multi-tasking, and are detail oriented we would like to speak with you about joining our team! We are looking for candidates who demonstrate professionalism and are interested in building relationships, challenging themselves to meet established goals, and providing a quality work product. Job Summary: Responsible for collecting and transmitting data gathered from designated retail stores primarily using a hand-held scanning
Experienced Regional Clinical Research Associates are being sought for one of the top large pharmaceutical companies in the world! Supporting new drug applications, the Regional CRA monitors clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines, and company SOPs. As specified in the monitoring plans, you will support project teams in the placement, implementation, evaluation, and conclusion of clinical studies. This role lets you use your exceptional interpersonal and communication
Kforce Clinical Research Staffing|Oklahoma City, OK|
Responsibilities: Experienced Regional Clinical Research Associates are being sought for one of the top large pharmaceutical companies in the world! Supporting new drug applications, the Regional CRA monitors clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines, and company SOPs. As specified in the monitoring plans, you will support project teams in the placement, implementation, evaluation, and conclusion of clinical studies. This role lets you use your exceptional interpersonal
Kforce Professional Staffing|Oklahoma City, OK, 73101|>3
Experienced Regional Clinical Research Associates are being sought for one of the top large pharmaceutical companies in the world! Supporting new drug applications, the Regional CRA monitors clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines, and company SOPs. As specified in the monitoring plans, you will support project teams in the placement, implementation, evaluation, and conclusion of clinical studies. This role lets you use your exceptional interpersonal and communication
Worldwide Clinical Trials|West Coast, North East and Mid West, OK|8
LOCATION: North America- West Coast, North East, and Midwest SUPERVISOR: Director, Clinical Operations North America SUMMARY: I Pre-Study Period A. Tasks Identify potential investigators for studies to be initiated. Participate in pre-study and study initiation visits. Ensure completeness and compile regulatory documents (e.g. IRB approval, informed consent, lab certification etc.). Coordinate study material
Pearson is an international media company with market-leading businesses in education, business information and consumer publishing. Pearson's education business represents about two-thirds of the company, and Penguin publishing and the Financial Times make up the balance. With more than 30,000 employees based in 60 countries, we are a family of businesses that draws on common assets, processes and shares a common purpose: to help our customers live and learn. Pearson is an Equal Opportunity Employer M/F/V
MODIS is searching for skilled, dedicated IT professionals to join our team. We always seek to deliver competitive and sought-after career opportunities to our potential consultants and employees. We are currently seeking a Research Engineer for our client in Midwest, OK. We invite you to review the position requirements below and apply today if your skills match our need. Position Type: Contract Skills Required: 3-4 years experience in all elements of software lifecycle, especially requirements
PacifiCare Health Systems, Inc.|Locations US-OK-Oklahoma City US-OK-Tulsa Organization i3 Clinical Monitoring Schedule Full-time
Additional Information Posting Date 07/11/2008, 07:07 PM, Montreal, New York, Washi|>4
Qualifications - Bachelor's level degree in life sciences, pharmacy, nursing or RN preferred - 4+ years of experience in clinical research, that includes 3+ years in clinical monitoring - Experience in Neuroscience - Thorough knowledge of all aspects of clinical research processes - Mastery of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements - Interpersonal savvy to ensure positive team and sponsor relationships - Demonstrated ability to work independently in performing