Clinical Pharmacist - Operations Manager
aplique agora
Localizações: Acra, Greater Accra Region
Full time
R1439757
Job description
Job Description Summary
Job Overview
• Supports and manages relationships with pharmacies in global clinical trials up to Phase III with a special focus on clinical trials conducted in the region
• Contact for IMP-related and Clinical Trial Supply Management (CTSM) -related questions for CROs/ Sites / pharmacies
• Contributes to training CROs and site personnel on IMP handling
• Liaises with GCP QA and supports CTSM GCP related activities
• Supports on appropriate CTSM GCP risk communication and ensures CTSM GCP requirements are met
• Manages complaints, deviations, changes, and other quality incidents for GCP topics
• Travel requirement: 15%
Qualifications
• Relevant professional experience (usually +3 years) in Clinical Supply or Clinical Research in Pharmaceutical/Biotech industry or CRO setting or any equivalent e.g., Pharmacy Services
• Relevant completed university education in Pharmacy, experience as a Clinical Pharmacist or in an equivalent role
• Deep understanding of country-specific requirement and standards for Clinical Trials conducted in the region
• Deep Knowledge about Pharmacy Manuals / Pharmacy Questionnaires
• Deep Knowledge about GCP principles (e.g., Ethical Principles, Adequate Drug Information, etc.)
• Business-professional English and local language skills
• Self-motivated with strong problem-solving and learning skills
• Ability to create independent analyses and develop new solutions
• Excellent organizational and communicative skills
• Enjoys working in a team
• Openness to explore on new topics for setting up the trend
• Supports and manages relationships with pharmacies in global clinical trials up to Phase III with a special focus on clinical trials conducted in the region
• Contact for IMP-related and Clinical Trial Supply Management (CTSM) -related questions for CROs/ Sites / pharmacies
• Contributes to training CROs and site personnel on IMP handling
• Liaises with GCP QA and supports CTSM GCP related activities
• Supports on appropriate CTSM GCP risk communication and ensures CTSM GCP requirements are met
• Manages complaints, deviations, changes, and other quality incidents for GCP topics
• Travel requirement: 15%
Qualifications
• Relevant professional experience (usually +3 years) in Clinical Supply or Clinical Research in Pharmaceutical/Biotech industry or CRO setting or any equivalent e.g., Pharmacy Services
• Relevant completed university education in Pharmacy, experience as a Clinical Pharmacist or in an equivalent role
• Deep understanding of country-specific requirement and standards for Clinical Trials conducted in the region
• Deep Knowledge about Pharmacy Manuals / Pharmacy Questionnaires
• Deep Knowledge about GCP principles (e.g., Ethical Principles, Adequate Drug Information, etc.)
• Business-professional English and local language skills
• Self-motivated with strong problem-solving and learning skills
• Ability to create independent analyses and develop new solutions
• Excellent organizational and communicative skills
• Enjoys working in a team
• Openness to explore on new topics for setting up the trend
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
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