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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.
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    • Excellent analytical skills with experience interpreting healthcare or clinical research data.
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    • Support the UK RPP in maintaining an effective pharmacovigilance system in compliance with MHRA requirements.
    • Assist in ensuring continuous oversight of all PV…
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    • Assist in clinical trial support when required.
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    • Supporting clinical assessment projects within key hospital accounts.
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    • Experience supporting clinical trials and negotiating Clinical Trial Agreements.
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    • Provide highly specialised clinical advice to the pharmacy clinical trials team regarding haematology and oncology trials conducted within the Trust.

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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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