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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Pharmaceutical Services Specialist
Job ID R0000038761 Harrow, England, United KingdomAs a Pharmaceutical Services Specialist, you will assist in the conduct of Phase I studies within the Pharmaceutical Services area in accordance with ICH Good Clinical Practice (GCP) and following local regulatory requirements and relevant Standard Operating Procedures (SOP’s).
You will participate in the assembly /dispensing of Investigational Medicinal Product (IMP) in accordance with written instruction and in compliance with Good Manufacturing Practice (GMP).
You will also manage assigned studies and are responsible for Pharmacy set up and delivery from start to end
Key Accountabilities:
Maintain drug accountability records in accordance with agreed protocols and the principles of International Conference on Harmonization Good Clinical Practice and Good Manufacturing Practice (Assembly (Manufacture, Packaging and Dispensing) of drugs in accordance with written instruction and in compliance with GMP
Prepare production worksheets and labels for assembly activities
Participate in IMP assembly activity
Responsible for assigned housekeeping tasks
Responsible for Pharmacy set up and delivery for assigned studies
Ensure controlled storage of all drugs (including controlled drugs, licensed drugs and unlicensed drugs) and materials sourced or supplied by sponsors for use in clinical trial studies
Ensure PS facilities (Assembly and storage areas) are maintained in compliance with regulatory requirements
Assist with investigation of quality incidents and deviations and ensuring corrective actions are completed.
Assist with audits (internal/ external) GMP
Knowledge, Skills & Experience
Preferably experience of working within the pharmaceutical industry, a Clinical Research Organization (CRO), Phase 1 clinical trial unit, or a hospital pharmacy setting.
Experience with Clinical Trial Supplies (Manufacture and Packaging)
Experience with batch assembly/ manufacturing of IMP/NIMP
Injection/infusion preparation experience and aseptic skills advantageous
Great communication skills
Must have good attention to detail
Enjoy working in a team
Adaptability
Education
Degree in Pharmacy, Pharmaceutical Science, Biology, Chemistry, or life science
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