Specialist Pharmacy Technician - Clinical Trials inSouthampton inSouthampton PUBLISHED
TUE 14 JAN 2025
Key responsibilities include supporting the dispensing of clinical trial prescriptions, checking prescriptions after obtaining ACPT qualification, and maintaining effective communication with Clinical Research Associates and organisations. Ideal candidates should be strong team players with a friendly demeanor, the ability to handle tight deadlines, and the capability to quickly understand complex information.
University Hospital Southampton NHS Foundation Trust is delighted to offer a fantastic opportunity to work with us.
Please see below for a detailed job description for the role.
An exciting opportunity has arisen for anenthusiastic and motivated band 4/5 pharmacy technicians to work as part of our pharmacy clinical trials team here at University Hospitals Southampton NHS Foundation Trust. Experience and knowledge of ICH good clinical practice and being a current holder of ACPT accreditation would be an advantage but is not essential.These permanent posts require specialist training in GCP and IMP management. You will work as a Senior Technician in Clinical Trials Pharmacy and must be committed to providing the highest quality of research and care for patients in all specialities.
Attached you will find the person specification document which provides more detail about the essential and desirable skills and experience needed for this role. We highly recommend you review this document and use it when completing your application as these criteria are used by hiring managers as guidance during shortlisting.
For an overview of the main duties of the role please see the 'Job Description and Main Responsibilities' section below. To understand the day-to-day responsibilities in more detail please read the full job description document attached.
About us
You will be responsible in setting up trials, ensuring that trials run smoothly; this will include accurate record keeping and drug accountability of clinical trials, reviewing protocol specific guidelines and liaising within a multi-disciplinary team.
You will need to be able to multitask, possess excellent communication skills, meet tight deadlines and thrive in a busy office.
Your Responsibilities
What youll do Support dispensing of clinical trials prescriptions Once ACPT qualified; support checking of clinical trials prescriptions Setup of assigned clinical trial studies Follow site procedure accurately of set up accurately and promptly Liaise with Clinical Research Associate/Organisation (CRA/CRO) to fulfil workflow tasks need for each assigned study in set up Following up in a timely manner on all queries with Clinical Research Associate/Organisation (CRA/CRO) Efficient production of study site file documentation
What were looking for A strong team player. Friendly and approachable manner. Polite, sympathetic, patient and diplomatic Proven ability to work to deadlines, prioritise and multi-task Able to learn and assimilate complex information quickly.
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