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Clinical Trials jobs in Buckinghamshire

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    • Knowledge of GCP guidelines and regulatory requirements pertinent to clinical trials.
    • The successful candidate will be responsible for overseeing and…
    • Develop new vitro models and pre-clinical activities to explore efficacy of new ImmTAAI effector molecules.
    • To conduct and design experimental investigations…
    • The ideal candidate will have experience in managing a diverse workload and possess in-depth knowledge of research governance and regulatory compliance and have…
    • At least 3 years of experience or understanding of clinical study start-up requirements and activities, showing your expertise in the field.
    • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
    • Experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.
    • Support the UK RPP in maintaining an effective pharmacovigilance system in compliance with MHRA requirements.
    • Assist in ensuring continuous oversight of all PV…
    • Understands the clinical impact of antibody and multi-specific-based therapies.
    • Liaise with Therapy area leaders and the drug pipeline-focused teams to identify…
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    • Supporting clinical assessment projects within key hospital accounts.
    • Supporting product evaluations, trials and implementation activities.
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    • Assist in clinical trial support when required.
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    • Strong understanding of GxP, regulated processes and the end-to-end clinical trial lifecycle.
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    • Experience supporting clinical trials and negotiating Clinical Trial Agreements.
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    • Provide statistical expertise for design, analysis and reporting of clinical trials and research projects.
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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

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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