Skip to main content
Post your CV and find your next job on Indeed!

Clinical Research Assistant jobs

Sort by: -
    • Is comfortable working in a fast-paced clinical research environment.
    • Support clinical trial sample processing activities.
    • Clinical trials : 2 years (required).
  • View similar jobs with this employer
    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • View similar jobs with this employer
    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • View similar jobs with this employer
    • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference…
  • View similar jobs with this employer
    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • View similar jobs with this employer
    • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference…
  • View similar jobs with this employer
    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • View similar jobs with this employer
    • You have successfully managed multiple clinical trial protocols across diverse investigative sites.
    • IQVIA has access to significant data pools allowing better…
    • Proven experience in patient care, preferably within a research or clinical setting.
    • No experience necessary, would suit a nurse looking to break into clinical…
    • Clinical operations or central lab logistics: 1 year (required).
    • This role oversees operational logistics for clinical trial drug supply and laboratory samples.
    • Research design and methods in clinical or social settings.
    • Higher degree/formal study of research design and methods in clinical or social settings.
    • Generous time off – 23 days of annual leave to recharge and unwind.
    • Document control, to include study-specific and general documentation.
    • Skills: Although we do not require prior professional research experience, an interest in carrying out research and a basic understanding of research techniques…
    • Advises staff and researchers, acting as a knowledgeable resource on matters relating to clinical practice and research, promoting an active and effective…
    • Postgraduate degree or equivalent from a premier B-school with proven work experience in research or professional services.

People also searched:

clinical trial
full time
graduate
healthcare
laboratory
medical
museum
part time
personal assistant
psychology

Job Post Details

Bank Clinical Laboratory Technician - job post

RDL Scientific Ltd
Cambridge
£21.25 - £29.11 an hour - Part-time
Responded to 75% or more applications in the past 30 days, typically within 1 day.

Job details

Pay

  • £21.25 - £29.11 an hour

Job type

  • Part-time

Location

Cambridge

Full job description

About the Role

We are seeking an experienced and motivated laboratory professional to join our Clinical Processing Laboratory team on a bank staff basis. This role will support clinical trial sample processing activities within a highly regulated GCP/GLP laboratory environment.

The successful candidate will play a key role in ensuring laboratory processes are performed in compliance with GSK procedures, ICH GXP standards, and HTA requirements, while delivering high-quality, regulatory-compliant data.

Key Responsibilities

  • Conduct laboratory processes in accordance with current policies and procedures
  • Work within ICH GXP and HTA regulatory frameworks
  • Support clinical trial sample processing activities
  • Follow Clinical Study Protocols and Study Reference Manuals accurately
  • Ensure all laboratory documentation and records are maintained to a high standard
  • Deliver regulatory-compliant data in line with organisational expectations
  • Adhere to Standard Operating Procedures (SOPs) and laboratory best practices

What We’re Looking For:

Essential Requirements:

  • Degree in a Biological Science discipline (minimum 2:1 or equivalent)
  • Minimum 2 years’ experience working within a regulated laboratory environment (GCP/GLP)
  • Minimum 2 years’ experience working in a clinical trials environment
  • Experience working with Clinical Study Protocols and Study Reference Manuals
  • Strong attention to detail and organisational skills
  • Ability to work independently and as part of a collaborative team

About You:

  • Understands the importance of compliance and accuracy
  • Is comfortable working in a fast-paced clinical research environment
  • Can follow detailed procedures and protocols consistently
  • Takes pride in maintaining high laboratory standards

Pay: £21.25-£29.11 per hour

Education:

  • Bachelor's (required)

Experience:

  • regulated laboratory : 2 years (required)
  • clinical trials : 2 years (required)

Work Location: In person

Let Employers Find YouUpload Your Resume