better Biotech Pharma Job in Iowa

Clinical Staff Pharmacist job in Rock Island IA Job Location Rock Island Iowa Category Pharmacy Staff Pharmacist Apply Now... Back to Results Soliant Health is now featuring travel opportunities in Iowa...

Biostatistician Req Number: mons-00008839 Location(s): Ankeny IA Responsibilities: The Crop Biometrics team seeks a biostatistician to evaluate the performance of crops with biotech traits and their dependence on crop genotypes in large-scale agricultural field trials. The biostatistician will: Coordinate the design and analysis of large-scale agricultural field trials Evaluate the equivalence of plant varieties with and without biotech traits to ensure

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

JOB DESCRIPTION SUMMARY: Serves as the primary liaison between Catalyst Rx Clinical Operations and Customer Service; provides clinical support to Client Services, Operations, IT and Customer Service Pharmacy Technicians, claims processing system, and plan development as it relates to clinical operations; and functions as a Clinical account manager for assigned client accounts. ESSENTIAL FUNCTIONS: Provides superior clinical consultation and account management with focus on client

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