Richmond Pharmacology
Clinical Trials Associate
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Department: Operations
Location: Richmond Pharmacology HQ
Compensation: £27,000 / year
Description
Title: Clinical Trials Associate
Location: London Bridge, London
Term: 12-month FTC, Full Time
Salary: £27,000 + Benefits (Private Medical, Private Dental, Pension, 25 days Annual leave plus bank holidays & many more)
A new opportunity has opened at Richmond Pharmacology for a Clinical Trials Associate to join a specialised team providing clinical support to Research Physicians and volunteers taking part in the trials of innovative new therapies. This is an entry level role with a career path focused on development of clinical excellence in the delivery of a variety of Phase I-III clinical trials.
Key tasks will include specific clinical procedures, ward rounds, ward maintenance, volunteer support and document management. Full training will be provided and candidates will be expected to pass assessments for key skills and maintain these to a high standard throughout.
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Main Duties And Responsibilities
- Previous experience working as a Healthcare Assistant
- Excellent communication skills and an engaging manner
- High energy, proactive and enthusiastic
- High attention to detail
- Available to work shifts (early, standard, late, night) including occasional weekends
- Customer service or hospitality sector experience would be attractive
- Successful candidates will need to pass DBS checks
Key Tasks
- Clinical - phlebotomy, ECG, vitals etc - training in all procedures provided
- Documentation - study specific documents, from point of collection to quality checking
- Sample collection - efficient, safe collection of samples from volunteers including accurate labelling and management
- Volunteer support - looking after the needs and monitoring the safety of volunteers within the ward environment – Immediate Life Support (ILS) training provided
- Ward maintenance - ensuring the wards are clean, tidy and properly stocked for the care of volunteers
- Queries - raising queries and assisting in the resolution of queries to ensure study requirements are delivered appropriately
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As well as working daily with volunteers, you will need to interact effectively with all other departments internally and provide an efficient service to support the delivery of clinical trials. You will need to familiarise yourself with all SOP's for working within the business, as well as all details specific to the trials you will be working on. This is a physically demanding and intellectually challenging role and represents an excellent opportunity to learn and develop a comprehensive range of clinical and scientific skills. Development will incorporate all elements of working in a clinical environment including QC and Scheduling and will lead to progression along a clinically specialised career path.
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