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Clinical Trial jobs in Hammersmith

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    • Knowledge of GCP guidelines and regulatory requirements pertinent to clinical trials.
    • The successful candidate will be responsible for overseeing and…
    • MUST HAVE: Experience in clinical trials..
    • Patient Assessments:* Perform clinical and cognitive assessments as required by trial protocols (e.g., MMSE, MoCA,…
    • Clinical research background - involvement clinical trials and research papers.
    • Clinical Evaluation Specialist - Radiology/Imaging A client of mine, a…
    • Exposure to clinical trial or quality improvement projects.
    • Coordinating clinical project delivery, from initiation through to completion.
    • Collaborate and work closely with clinical supervisors to adapt and refine therapy plans for effective, engaging support.
    • A laptop to use in work and at home.
    • 2/ Build senior clinical and digital relationships — establish trusted advisor status with CIOs, CMIOs, CCIOs, and transformation leads across target accounts,…
    • Strong working knowledge of the clinical drug development process with experience in the conduct/participation of clinical trials (investigator initiated,…
    • Support induction and clinical training of new staff.
    • Experience leading small teams and delivering clinical training.
    • BCBA and/or UKBA(cert) certification.
    • GHO drives the demonstration of value for ViiV medicines, optimizing patient benefit and access, with a growing focus on Real World Evidence (RWE) and Patient…
    • Technical Mastery: Extensive understanding of end-to-end pharmacovigilance processes, including Deviation/CAPA management and the conduct of clinical research.
    • Experience working alongside SALT, OT, or clinical teams.
    • September 2026 or Jan 2027 start. .
    • Salary:* £44,238 - £52,300 (dependent on experience).
    • Demonstrated experience leading innovative trial designs, including adaptive designs and decentralized clinical trials (DCTs); learning agility to support…
    • Experience supporting clinical trials and negotiating Clinical Trial Agreements.
    • Support local and global R&D teams with clinical trial regulations and…
    • Advise teams on clinical trials, including reviewing and negotiating agreements.
    • £450 - £580 per day PAYE or £595.96 - £768.13 per day Umbrella.
    • Design and run global real-world evidence (RWE) studies from concept through to publication.
    • Work on a collaborative study with an academic partner to grow a…

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Job Post Details

Clinical Research Coordinator - job post

Velocity Clinical Research, Inc.
Desborough Road, High Wycombe HP11 2QW
£30,000 - £40,000 a year - Full-time
Responded to 75% or more applications in the past 30 days, typically within 1 day.

Job details

Pay

  • £30,000 - £40,000 a year

Job type

  • Full-time

Location

Desborough Road, High Wycombe HP11 2QW

Benefits

Pulled from the full job description

  • Referral programme
  • Employee discount
  • Sick pay
  • Free parking
  • Company pension
  • Health & wellbeing programme
  • Enhanced maternity leave

Full job description

Job Overview
We are seeking a dedicated Clinical Research Coordinator to join our dynamic research team. The successful candidate will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulatory standards, and maintaining accurate documentation. This role offers an excellent opportunity for individuals passionate about advancing medical science and improving patient outcomes. The position is paid and suitable for candidates with a keen eye for detail, organisational skills, and a strong interest in clinical research.

Responsibilities

  • Coordinate and manage all aspects of clinical trials, including participant recruitment, scheduling, and follow-up.
  • Ensure adherence to study protocols, regulatory requirements, and ethical standards.
  • Collect, record, and maintain accurate trial data in accordance with Good Clinical Practice (GCP) guidelines.
  • Liaise with investigators, healthcare professionals, and study participants to facilitate smooth trial operations.
  • Monitor participant safety and report adverse events in compliance with regulatory procedures.
  • Prepare and submit necessary documentation to ethics committees and regulatory authorities.
  • Assist in training new staff or interns involved in the research projects.
  • Maintain organised records of all trial-related documentation for audit purposes.

Requirements

  • Bachelor's degree in health sciences, nursing, or a related field; relevant experience in clinical research is preferred.
  • Strong organisational skills with the ability to manage multiple tasks efficiently.
  • Excellent communication skills to liaise effectively with team members, participants, and external agencies.
  • Knowledge of GCP guidelines and regulatory requirements pertinent to clinical trials.
  • Ability to work independently as well as part of a multidisciplinary team.
  • Proficiency in data management software and Microsoft Office Suite.
  • Attention to detail and high level of accuracy in documentation.
  • Prior experience working within healthcare or research environments is advantageous but not essential. This role provides an engaging environment for professionals committed to advancing healthcare through meticulous research practices while contributing meaningfully to medical progress.

Job Type: Full-time

Pay: £30,000.00-£40,000.00 per year

Benefits:

  • Company pension
  • Employee discount
  • Enhanced maternity leave
  • Free parking
  • Health & wellbeing programme
  • Referral programme
  • Sick pay

Work authorisation:

  • United Kingdom (required)

Work Location: In person

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