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

Clinical Research jobs in Wiltshire

Sort by: -
  • View similar jobs with this employer
    • Experience working with clinical or research partners to support collaboration and study delivery.
    • Experience training research staff or site teams.
    • Refer participants for respective clinical trials where appropriate.
    • Provide medical oversight on clinical trial conduct at allocated site.
  • View similar jobs with this employer
    • Provide technical and clinical support during surgical procedures.
    • Serve as a trusted clinical resource to customers, answering questions and demonstrating best…
    • Provide clinical care for research participants within the boundaries of own knowledge, competence, and skill level.
    • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference…
    • Part-Time Field Interviewer – Office for National Statistics (ONS)*.
    • Visiting pre-selected households chosen through a statistical sample (not volunteers).
    • Refer participants for respective clinical trials where appropriate.
    • Provide medical oversight on clinical trial conduct at allocated site.
    • Refer participants for respective clinical trials where appropriate.
    • Provide medical oversight on clinical trial conduct at allocated site.
    • Refer participants for respective clinical trials where appropriate.
    • Provide medical oversight on clinical trial conduct at allocated site.
    • Refer participants for respective clinical trials where appropriate.
    • Provide medical oversight on clinical trial conduct at allocated site.
    • Refer participants for respective clinical trials where appropriate.
    • Provide medical oversight on clinical trial conduct at allocated site.
    • Interprets multi-source clinical and safety data to develop evidence-based conclusions.
    • Provides expert peer review and mentorship to Specialists and Associate…
    • The role leads the delivery of research and information outputs for a defined group of member banks and insurers, with a strong focus on effective facilitation,…
    • Familiarity with public health principles and clinical research methodologies.
    • Engage in clinical research and contribute to public health initiatives as…

People also searched:

clinical trial

Job Post Details

Trials Manager - job post

University of Bath
4.1 out of 5 stars
Bath BA2
£38,784 a year - Part-time, Fixed term contract
You must create an Indeed account before continuing to the company website to apply

Job details

Pay

  • £38,784 a year

Job type

  • Fixed term contract
  • Part-time

Location

Bath BA2

Full job description

Trials Manager

Department
Institute for Augmented Human

Salary
Starting from £38,784, rising to £46,049 pro rata per annum

Closing date
Monday 20 July 2026

The Bath Institute for the Augmented Human (IAH) is an ambitious interdisciplinary research institute at the University of Bath, bringing together expertise from engineering, neuroscience, healthcare, computer science, psychology, and design to develop technologies that enhance human capability and wellbeing.

The Research Trials Manager plays a pivotal role in enabling these innovations to be tested safely, ethically, and effectively through high-quality research involving human participants.

About the role

This role is central to the successful delivery of trials evaluating emerging technologies such as neurotechnology, wearable systems, augmented and virtual reality, AI-driven digital assistants, and assistive devices such as exoskeletons. These technologies have the potential to improve physical and cognitive performance, health outcomes, and quality of life. The Trials Manager will help transform innovative concepts into robust clinical and real-world evidence through well-designed and carefully managed trials.

Working closely with academic investigators, clinicians, regulatory bodies, and research participants, the postholder will support the design, setup, and delivery of trials across multiple sites, including NHS environments. This includes ensuring that all studies meet Good Clinical Practice (GCP) standards and regulatory requirements, managing approvals and documentation, and coordinating recruitment and participant engagement activities.

Key areas of focus include:

- Delivering high-quality research trials: Coordinate and manage trials involving human participants across multiple sites, ensuring compliance with regulatory and governance requirements.
- Supporting study design and approvals: Assist with developing protocols, obtaining ethical and regulatory approvals, and preparing participant-facing documentation.
- Managing multi-site collaboration: Work closely with clinical partners, NHS teams, and research staff to ensure effective recruitment and delivery of studies.
- Driving participant engagement and recruitment: Support recruitment strategies, identify risks to delivery, and contribute to solutions that maintain trial progress.

The role involves working across different environments, including university laboratories, NHS settings, and partner organisations, and may require travel to support trial delivery and staff training. The Trials Manager will also contribute to knowledge sharing across the Institute, helping to establish best practices in trial design and delivery and strengthening the Institute’s capability to conduct impactful research.

This is an exciting opportunity for an individual with experience in clinical or human-participant research who is motivated to support innovative technologies and interdisciplinary collaboration. The role offers the chance to contribute to research that shapes future healthcare and technology solutions.

We are seeking a motivated and organised individual with experience supporting or managing research involving human participants. You will be comfortable working across multiple stakeholders and environments, with strong attention to detail and a commitment to research quality and regulatory compliance.

About you

A higher degree in a relevant subject with experience in trials management, or equivalent relevant experience and professional qualification.

- Experience working in research involving human participants, including coordinating study delivery or data collection
- Demonstrated knowledge of Good Clinical Practice (GCP), GDPR, and the UK Policy Framework for Health and Social Care Research
- Experience supporting or managing ethical approval processes for research studies
- Experience collecting, managing, and handling data from multiple participants or large datasets
- Experience working with clinical or research partners to support collaboration and study delivery
- Strong written and verbal communication skills, including preparing reports and communicating with diverse stakeholders
- Ability to work independently, manage priorities, and deliver tasks to agreed timelines
- Strong IT skills relevant to research coordination and data management
- Commitment to working within professional and ethical research standards

Desirable qualifications and experience

- Experience obtaining regulatory approvals (e.g., MHRA approvals)
- Experience supporting multi-site trials, particularly involving NHS partners
- Experience supporting recruitment strategies and participant engagement activities
- Experience contributing to the preparation of research protocols or grant applications
- Experience training research staff or site teams
- Experience presenting findings or contributing to dissemination activities such as conferences or workshops

Key attributes

- Highly organised with strong attention to detail
- Proactive and solution-focused, particularly when addressing recruitment or delivery challenges
- Collaborative team member with strong interpersonal skills
- Resilient and adaptable, able to manage competing priorities
- Committed to high-quality research delivery and participant safety

Further information

This is a part-time (18.25 hours per week), fixed term role from September 2026 to July 2030.

We're very proud to be a signatory of the Armed Forces Covenant, an accredited Disability Confident Leader, and an autism friendly university, committed to building disability confidence and supporting disabled staff.

What we can offer you

We're continually expanding our benefits package to better support you and enhance your experience with us. The list found via the apply button is just an example of some of the many great benefits we offer.

Pay: £38,784.00 per year

Work Location: In person

Let Employers Find YouUpload Your Resume