Clinical Trials Associate

2 weeks ago

London, United Kingdom Richmond Pharmacology Full time

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)

Richmond Pharmacology are an early phase Clinical Research Organisation (CRO), where we are conducting pioneering early phase healthy participants and patient participant trials. Our experienced and world-renowned team, our central London location and our global reach contribute to making Richmond Pharmacology an exciting and dynamic place to work.

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.

**Requirements**:

- 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

**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

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.

**Application

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