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AMS Advanced Medical Services

Clinical Research Associate (CRA) – West London

London
Posted about 15 hours ago
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AMS Advanced Medical Services Ltd.

AMS Advanced Medical Services Ltd. is a full-service Clinical Research Organisation providing support to the Pharmaceutical and Biotechnology industries across Europe with groundbreaking phase I-IV Global Clinical Trials in Rare Diseases and other indications. With a great team based in West London, there has never been a more exciting time to join us!

Role Overview

We are looking for a Clinical Research Associate (CRA) with 1-2 years’ experience, to be based in our Hammersmith office (part-time or remote working will be considered for the right applicant), monitoring sites across UK and Ireland. You will be involved in the whole trial process from Site Selection, through Site set-up, monitoring and close down. The position is very varied and hands-on, you could be working in any Phase of Clinical Development or Disease Area including trials with Medical Devices and Non-interventional studies.

Responsibilities

As a Clinical Research Associate at AMS Advanced Medical Services Ltd, you will:

  • Study start-up: Help with feasibility questionnaires, contacting potential study sites, and participate in site selection in close collaboration with Project Managers and Sponsors.
  • Regulatory compliance: Coordinate with Project Managers and study sites to collect and review essential site documents to ensure that all requirements are met on time for regulatory submissions.
  • Study site management: Support site activation, ongoing site management, site training, including monitoring activities from feasibility to close-out, in line with GCP, SOPs, study protocols, and plans.

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Required Experience

  • Education: Bachelor’s degree in Life Sciences, Nursing, Pharmacy, Medical Science, Public Health, or equivalent.
  • Clinical research experience: Minimum of 1–2 years’ experience as a Clinical Research Associate (CRA), with hands-on involvement in site initiation, Investigator Site File (ISF) management, and site monitoring for clinical and/or non-interventional studies.
  • Communication skills: Excellent written and verbal English proficiency (at least C1-C2 level). Proficiency in additional languages is a strong advantage.
  • Technical skills: Proficient in MS Office and experienced with EDC, eTMF, and CTMS systems, with a strong aptitude and willingness to learn and manage multiple technical tools.
  • Personal competencies: Highly organized with strong problem-solving abilities, effective cross-cultural collaboration skills, a proactive mindset toward process improvement, teamwork, and the ability to manage multiple priorities in a fast-paced environment.
  • Attention to detail: Capable of working independently and in a team with a high level of accuracy, diligence, and thoroughness when executing complex tasks.

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Job Types

  • Full-time, Permanent

Benefits

  • Company pension
  • Life insurance
  • Private medical insurance

Education

  • Bachelor's (required)

Experience

  • Good Clinical Practice: 1 year (required)

Work Location

  • Hammersmith, London

Application

Are you interested? If you have the required experience for this position and are eligible to work in the UK then please apply to: Recruiting-Team@ams-europe.com with a Cover letter and CV.

We look forward to receiving your application!

Your AMS Recruiting Team

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Skills

Clinical Research
Site Monitoring
Regulatory Compliance
Communication Skills
Problem Solving
Teamwork
Attention to Detail
Technical Skills
MS Office
EDC
eTMF
CTMS
Life Sciences
Nursing
Pharmacy
Medical Science

Location

London, England, United Kingdom

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