Skip to main content
Post your CV and find your next job on Indeed!

Health Practice jobs in Wallingford

Sort by: -
    • This role provides an engaging environment for professionals committed to advancing healthcare through meticulous research practices while contributing…
    • To help maintain high clinical standards in all areas of the practice and follow SOPs/practice protocols.
    • To help maintain practice appearance.
    • Must have a minimum of two years post registration experience in PHC practice.
    • Child Health in Primary Care (only if working in a families practice as…
    • Assisting the Laboratory Supervisor to ensure an efficient service to the customer at all times, including giving feedback and suggestions on working practices.
    • View all UK Health Security Agency jobs - Didcot jobs - Laboratory Technician jobs in Didcot
    • Salary Search: PDS Process Laboratory Technician (Bank) salaries in Didcot
    • See popular questions & answers about UK Health Security Agency
    • Excellent working knowledge and demonstrable understanding of relevant legislation, policy, technical guidance and industry standards and best practice relating…
    • The post-holder will be required to keep fully up-to-date with their relevant area of practice and to demonstrate this as part of the annual appraisal process.
    • Regular supervision and reflective practice.
    • Knowledge or experience of attachment-informed practice, Dyadic Developmental Psychotherapy (DDP), trauma-informed…
    • Driving continuous improvement, innovation and the adoption of best practice.
    • A relocation package may be available (terms and conditions apply).
    • Strong knowledge of food safety practices and hygiene standards.
    • Follow all health and safety protocols to prevent cross-contamination and ensure a safe…
    • Postgraduate qualifications in women's health (e.g., DRCOG or DFSRH).
    • This is an exciting opportunity for a GP who is looking to develop and expand their…
    • Working autonomously, the ACP will deliver safe and effective care within agreed local and national guidelines, drawing on advanced clinical reasoning and…
    • Champion a positive health & safety culture across all sites and levels of the organisation.
    • Ability to design and deliver engaging health and safety training…
    • Adhere to best practice guidance covering areas such as records management, data protection legislation and BACP ethical code of practice.
    • Sound knowledge of current Health & Safety legislation and best practices.
    • You’ll be a visible role model for your team, ensuring exceptional service delivery,…
    • The purpose of the Dual Site AD Food Processing Operative is reporting to the Site Managers for day-to-day operations and part of a rolling standby night rota,…

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

Let Employers Find YouUpload Your Resume