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Clinical Trial Assistant jobs in Surrey

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    • Experience with statistical software used for data analysis in clinical trials.
    • In this energetic position, you will support clinical trials by coordinating…
    • Key requirements: * Experience in patient care - 2+ years minimum * Experience in clinical evaluation, clinical data assessment, and medical statistics -…
    • Act as a recognised expert and professional role model within the clinical research environment, including direct and indirect clinical care, teaching, audit…
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    • Oversee recruitment, delivery, and follow-up activities for clinical trials.
    • Support the management and governance requirements of clinical research studies.
    • Coordinate own portfolio of clinical studies.
    • The portfolio includes both commercial and academic studies, encompassing observational and complex interventional…
    • Relevant MSc, or postgraduate qualifications in a clinical area.
    • Deliver high-level clinical care while supporting the team to maintain and develop practical…
    • Evaluate patient eligibility for clinical trial entry, co-ordinating pre-study tests, obtaining results and arranging appropriate appointments according to…
    • The position is ideally based in London or Birmingham with hybrid-working or office-based options.
    • Undertake research and analysis relating to healthcare policy…
    • The Alzheimer's Society UKDTN Lead Clinical Research Nurse is a senior clinical leadership role responsible for leading the delivery and development of early…
    • As an Alzheimer's Society UKDTN Senior Clinical Research Nurse, the post holder will provide clinical and administrative support to ensure effective delivery of…
    • You have successfully managed multiple clinical trial protocols across diverse investigative sites.
    • Perform site monitoring visits (selection, initiation,…
    • IQVIA provides scientific solutions spanning clinical trials, real world evidence, and consulting in all areas of the drug product lifecycle.
    • This part-time role is to support multiple clinical trials in London on a bank basis.
    • BS/BA in life sciences or educational equivalent and/or relevant work…
    • Experience supporting clinical trial regulatory submissions in the UK.
    • Collect, review, and prepare site and regulatory documentation required for UK clinical…
  • View similar jobs with this employer
    • Min of 2-3 years of experience working in clinical trials.
    • Master's degree in psychology, Psychiatry or a related field.

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Clinical Research Assistant
Velocity Clinical Research, Inc.
Arcadia Avenue, London N3 2JU
£30,000 - £35,000 a year
Fixed term contract
Apply now

Job details

Here’s how the job details align with your profile.

Pay

£30,000 - £35,000 a year

Job type

Fixed term contract

Full job description

Job Overview

Join our dynamic team as a Clinical Research Assistant and play a vital role in advancing medical knowledge through meticulous research and patient care. In this energetic position, you will support clinical trials by coordinating activities, monitoring patient progress, and ensuring compliance with regulatory standards. Your enthusiasm and attention to detail will help drive innovative healthcare solutions forward while providing exceptional support to research teams and participants alike. This paid position offers a unique opportunity to develop your expertise in clinical research within a collaborative and fast-paced environment.

Duties

  • Assist in the planning, setup, and execution of clinical studies, ensuring all procedures adhere to FDA regulations and Good Clinical Practice (GCP) standards
  • Monitor patients throughout the study, recording vital signs, administering tests, and tracking adverse events to ensure safety and protocol compliance
  • Maintain accurate data entry and management using statistical software and specialized data management systems
  • Prepare and organize study documentation, including consent forms, case report forms, and regulatory submissions
  • Support patient recruitment efforts by screening potential participants and explaining study protocols clearly
  • Conduct phlebotomy procedures when necessary, collecting blood samples following strict safety protocols
  • Collaborate with the research team to analyze data trends, prepare reports, and assist in interpreting results for ongoing studies

Experience

  • Prior experience in clinical research or healthcare settings is highly desirable
  • Strong understanding of medical terminology and clinical procedures
  • Demonstrated analysis skills for interpreting data accurately and efficiently
  • Experience with statistical software used for data analysis in clinical trials
  • Knowledge of FDA regulations, GCP guidelines, and compliance management practices
  • Supervising experience or nursing background is a plus for overseeing patient care activities
  • Proficiency in patient monitoring techniques, including vital signs assessment and documentation
  • Familiarity with data management systems used in clinical research environments

Join us to contribute meaningfully to groundbreaking health initiatives! We value proactive individuals who thrive on collaboration, precision, and making a difference in patient outcomes. This role provides an excellent platform to grow your career in clinical research while supporting innovative medical advancements.

Pay: £30,000.00-£35,000.00 per year

Work Location: In person

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