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Study Lead - Clinical Research

London   •  £30000 - £45000 per annum + + Benefits  •  Permanent, Full time

Study Lead - Clinical Research

Permanent Position - £30,000 to £45,000 annually

Based in Central London

Do you have a background in co-ordinating studies within a clinical research environment?

Would you like to work for a leading clinical research and development organisation with an ongoing COVID-19 project and exciting study pipeline?

Through their specialised clinical trial platform, my client plays a key role in drug and vaccine development across a range of infectious and respiratory diseases. Their state of the art clinical and laboratory facilities are based in Central London, where they are looking to bring on board a Study Lead - Clinical Research to provide direction and co-ordination of clinical study activities to ICH-GCP standards.

This is an excellent opportunity to join a team of driven clinical research professionals, within an organisation leading the way with their clinical trial platform and so playing a key role in drug discovery, development and COVID-19 advancements.

Key Responsibilities of the Study Lead - Clinical Research will include;

  • Assist in the evaluation of proposed clinical studies, advising on study design, objectives and strategic direction.
  • Co-ordination of clinical study activities from study set-up and screening through to follow up.
  • Serve as the clinical study team's internal point of contact for any study related communication and associated queries.
  • Act as the clinical protocol expert, providing guidance to the team and ensuring protocol compliance across the clinical site.
  • Frequently advise and update stakeholders on the study status, including at internal project meetings and with external sponsors.
  • Ensure studies are recorded and reported in accordance with standard operating procedures, good clinical practices and other applicable regulatory requirements.

To be considered for this Study Lead - Clinical Research vacancy you will need the following skills and experience;

  • BSc/MSc/PhD in a scientific subject (Biomedical Science, Biochemistry, Virology, Immunology, Molecular Biology, Cell Biology, Infectious Disease etc.) or equivalent working experience.
  • Experience within a clinical research environment; co-ordinating, leading or managing studies e.g. Study Manager, Study Lead, Clinical Research Associate, Clinical Trials Coordinator etc.
  • Demonstratable awareness of ICH-GCP and associated regulatory standards.
  • Able to plan and manage projects, providing regular reports and updates to ensure projects run to time and budget.
  • Excellent communication skills and a personable nature, to support relationship building with stakeholders and cross functional teams.
  • Strong written skillset in order to prepare technical scientific reports, documents and presentations.
  • Excellent organisation skills, with a 'self-starter' attitude.

Key Words "Clinical Research, Clinical Studies, Clinical Trial, Study Lead, Study Manager, Clinical Research Associate, CRA, ICH-GCP, Good Clinical Practice, GcP, GxP, Virology, Immunology, Biomedical Science, London"

Please apply online or call Katie-May Kress on 0203 0964711 for more information

You must have the right to work in the UK. Learn more

  • Agency: SRG
  • Contact: Katie-May Kress
  • Phone: 0203 096 4711
  • Reference: J33967
  • Posted: 8th November 2021
  • Expires: 6th December 2021


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