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  • biotechnology lab

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    Welcome to LR Clinical Solutions

    LR Clinical Solutions Limited provide a range of advice and support services to pharmaceutical, biotechnology and CRO companies.

    We believe that a satisfied client is one that will come back again, and our aim is to make that a reality.

  • Lab Work

    Choose Efficiency

    Committed to providing work of high quality!

    We focus on the key areas of planning, preparation and conduct of clinical trials from setting up through maintenance and closure of your studies. The company has a network of regulatory, QA and other industry associates to enable us to provide advice in a wide range of areas.

  • DNA

    Choose Commitment

    Highest professional standards

    We are committed to providing work of the highest quality, delivered on time, in full and to the highest professional standards. We ensure that we provide seamless continuity with your companies systems and operations.

Our core services

Clinical Operations

Leadership and management of clinical operations teams and research programmes.

Study Management

Clinical trials organisation and management, phases I to IV, single centre and multinational.

Medical Writing

Management of Clinical Study Report writing, Study design concept and Protocol preparation

Project Management

Clinical trial design, development and coordination.

About Us

lab testing

LR Clinical Solutions Limited is a clinical research consultancy with a difference, having a unique experience of working directly for CRO, biotech and blue-chip pharma companies, which allows us to have a global overview of the clinical process in every market environment.

We will work hand in hand with your organisation to ensure the smooth and successful running of your clinical trials and, crucially can hit the ground running to ensure the seamless continuation of your clinical programmes.

The Managing Director of the company, Dr Lutfat Rahaman, began her career in the pharmaceutical industry in 1993 working in data management for a CRO. She followed this with a move into clinical research, becoming a CRA and then rapidly progressing into project management.

  • Lutfat has been responsible for the project and/or programme management of key pharmaceutical and device products for biotechnology and pharmaceutical companies since 1997. Her experience includes managing large international, multi-centre projects from study concept to report writing as well as experience in the cross-functional management of trials using both internal and outsourced resource, as well as working on small Investigator Sponsored studies.
  • Lutfat has been offering her services as a freelance clinical project and programme manager through her own independent company, LR Clinical Solutions since 2007, working with several blue chip pharmaceutical and biotechnology companies.
  • Lutfat has worked in a variety of therapeutic areas, such as oncology, neuroscience, dental pain, asthma, obesity, renal transplants, psoriasis, haematology, intermittent claudication, gastroenterology, ophthalmic, diabetic foot, HIV and has worked both on the development of drugs and medical devices.
  • Lutfat has an honours degree in biochemistry and clinical biology from the University of Manchester, Institute of Science and Technology (UMIST) and a PhD in biochemistry from the University of London, Charing Cross and Westminster Medical School.

Our Services

  • Project management and clinical development planning

    • Proactive project management and tracking to achieve programme goals
    • Clinical trial design, development and coordination
    • Identification of experts, investigators, technologists for input to product development plans
    • Evaluation of current medical practice and potential market need
    • Coordination of advisory board meetings
  • Study Management

    • Study feasibility
    • Investigator site evaluation and selection
    • Coordination and management of cross-functional study teams
    • Clinical trials organisation and management, phases I to IV, single centre and multinational
    • Investigator meetings organisation, including the development and review of materials
    • Presentation at Investigator meetings
    • Management of production, packaging and labelling requirements for investigational medicinal product requirements
    • Design and organisation of investigational medicinal product supply
    • Coordination of data management and clinical data review
    • Review of data management and statistical analysis plans
    • Evaluation, selection and management of CROs and clinical and technical support services
    • Study tracking
  • Clinical Operations

    • Leadership and management of clinical operation teams
    • Line management of CTA's, CRA's and project managers
    • Evaluation, selection and management of CROs and clinical and technical support services
    • Outsourcing and contract negotiation
    • Budget and resource tracking and management
  • CRO Management

    • Development of request for proposals
    • Review of proposals, selection and evaluation of clinical and technical service providers
    • Management of clinical and technical service providers
  • Medical writing

    • Study design concept and Protocol preparation
    • Patient information leaflets
    • Ethics applications
    • Case Report Form design
    • Management of Clinical Study Report writing
  • Training and development

    • Good Clinical Practice training
    • Training of study personnel (e.g. investigators, study nurses/coordinators, CRAs, CROs, SMOs)
    • Investigator meetings

What our customers say

  • “Lutfat has a wealth of site and study management experience and is consistently poised, organized, and forward thinking in all of her interactions. It was a pleasure to work with Lutfat and I certainly hope to work with her again”

  • “Lutfat is a results orientated project manager, reliable and proactive in her approach to her daily activities. Her communication style had a positive effect on ensuring delivery and she was well respected by her peers and colleagues.”

  • "Lutfat is a team great player with high integrity and reliability. She has excellent communication skills and in depth knowledge of clinical trial program management. Her extensive experience in this area combined with her innovative working style puts her well above many others in this field. She has the ability to integrate quickly into the team and makes valuable contribution to the program.”

  • "Lutfat is an exceptionally well organised and competent clinical project manager. She is capable of both seeing the big picture and detailing with all the detail.”

    Contact Us


    • LR Clinical Solutions Ltd
      138 Canterbury Road, Harrow,
      Middlesex, HA1 4PB

    • +44 (0) 203 371 8231

    • +44 (0) 208 427 0736 (FAX)

    • +44 (0) 7748 188592

    • enquiries@lrclinicalsolutions.com