Clinical Research Associate – West London
Job Description
AMS Advanced Medical Services Ltd. is a full-service Clinical Research Organisation providing support to the Pharmaceutical and Biotechnology industries across Europe with ongoing and 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
We are looking for a 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 What you will do
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 on site selection in close collaboration with Project Managers and Sponsors.
* Regulatory compliance: Coordinate with PM and study sites collecting checking, collecting the core regulatory of 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.
Required Experience
* Education: Bachelor's degree in Life Sciences, Nursing, Pharmacy, Medical Science Public Health, or equivalent, with a minimum of one-year hands-on clinical research experience.
* Clinical research experience: Minimum of 1–2 years' experience as a Clinical Research Associate (CRA), with hands-on involvement in site initiation, Trial Master File (TMF) management, and site monitoring for both clinical and non-interventional studies.
* Communication skills: Excellent written and verbal English proficiency. Proficiency in additional languages is a strong advantage.
* Technical skills: Proficient in MS Office and experienced with EDC, BSI, 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, initiative in process optimization 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.
* Right to work in the UK
If you have the required experience for this position and are eligible to work in the UK then please apply to: Karla Lima with a Cover letter and CV.
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: In person