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Clinical Trials Associate

PharmiWeb.jobs: Global Life Science Jobs

London

On-site

GBP 27,000 - 32,000

Full time

30+ days ago

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Job summary

An exciting opportunity has arisen for a Clinical Trials Associate at a pioneering Clinical Research Organisation in central London. This entry-level role is perfect for individuals eager to develop their clinical skills while supporting innovative trials. You will engage with volunteers, assist in clinical procedures, and ensure the smooth operation of trial documentation. The position promises a dynamic work environment with full training provided, allowing you to grow in a supportive team. If you are energetic, detail-oriented, and passionate about healthcare, this role offers a fantastic career path in clinical excellence.

Benefits

Private Medical Insurance
Private Dental Insurance
Pension Plan
25 Days Annual Leave
Bank Holidays

Qualifications

  • Entry-level role with a focus on clinical excellence in Phase I-III trials.
  • Candidates must pass assessments for key skills and maintain high standards.

Responsibilities

  • Support Research Physicians and volunteers in clinical trials.
  • Conduct clinical procedures like phlebotomy and ECG.

Skills

Communication Skills
Attention to Detail
Proactive Attitude
Customer Service

Education

Healthcare Assistant Experience

Tools

Clinical Documentation
Immediate Life Support (ILS)

Job description

Title: Clinical Trials Associate

Company: Richmond Pharmacology

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

A new opportunity has opened for a Clinical Trials Associate to join a specialised team providing clinical support to Research Physicians and volunteers taking part in trials of innovative new therapies. This is an entry-level role with a career path focused on the development of clinical excellence in the delivery of a variety of Phase I-III clinical trials.

Key tasks will include:

  1. Specific clinical procedures, ward rounds, ward maintenance, volunteer support, and document management.
  2. Full training will be provided, and candidates will be expected to pass assessments for key skills and maintain these to a high standard throughout.

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
  • 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

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 SOPs 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:

If you are interested in the role, please register your details, including a copy of your CV. Please note, while we try to respond to every candidate, the high volume of applications anticipated may make this impossible and we ask for your patience and understanding. If you have not heard from us within two weeks of making your application, please assume that you have not been successful on this occasion.

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