better Biotech Pharma Job in Houston TX

Clinical Research Analyst Job Category: Managerial/Professional Sub Category: Research Department: Gynecologic Oncology Salary:SALARY_LOW=0; SALARY_LOW=46800.00; if(SALARY_LOW==0) document.write('Not Available'); else document.write('$46800.00 - $70200.00'); Employment Status: Full Time Work Week: Mon-Fri Shift: Days SUMMARY The primary purpose of the Clinical Research Analyst is to provide strategic planning and administration of payment monitoring for research studies sponsored by private industry

Clinical Research Program Coordinator Job Category: Research Sub Category: Professional Department: Gynecologic Oncology Salary:SALARY_LOW=0; SALARY_LOW=46000.00; if(SALARY_LOW==0) document.write('Not Available'); else document.write('$46000.00 - $69000.00'); Employment Status: Full Time Work Week: Mon-Fri Shift: Days Function: Provides administrative and patient care services for the coordination of clinical research activities for the Clinical Cancer Genetics Program. Scope: Coordinates clinical research

Clinical Research Coordinator Description: - Responsible for procuring, maintaining, and assuring protocol compliance for all patients on clinical trials. - Collaborates with physician in determining eligibility of patients for clinical trials. - Provides education for staff and patients. - Ensures site research quality by practicing in compliance with Corporate Policy and Procedures, ICH principles of Good Clinical Practice and applicable federal, state, and local regulations. -

SUMMARY The primary purpose of the Clinical Research Analyst is to provide strategic planning and administration of payment monitoring for research studies sponsored by private industry, foundations, and federal agencies for the Department of Gynecologic Oncology. SCOPE: Responsible for the financial management and oversight of all research protocol contracts. Assists faculty and Principal Investigators with the development and negotiation of financially appropriate contracts and budgets for research protocols

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