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

Clinical Research jobs in Leeds

Sort by: -
    • You will work alongside the wider clinical research team in the assessment and management of patient care pathways.
    • Annual Leave Buy and Sell Scheme.
    • 1 x permanent band 7 Clinical Scientist Bioinformatician position (based at either Leeds, Sheffield or Newcastle North East and Yorkshire Genomic Laboratory Hub…
    • Coordinating and managing Neurology clinical trials.
    • A proactive approach, attention to detail, commitment to high-quality data collection, and a passion for…
    • Their role will involve leadership and management for the clinical research workforce in this area, including developing and enhancing the capacity and…
    • At Senior level , you bring extensive Quality and Compliance experience from a GCP‑regulated clinical trials environment , such as a CRO or hospital research…
    • Maintain operational grip in a fast‑moving, live clinical research environment.
    • Plan and oversee daily pharmacy activity to support active clinical trials.
    • Ensuring all clinical trials are conducted according to Protocol, recruiting patients who are eligible for the study.
    • Annual Leave Buy and Sell Scheme.
  • View similar jobs with this employer
    • 1 or more years of experience in clinical research.
    • 1 or more years’ experience in leading database management, study design or global project management in…
    • Delivery of complex clinical trials exploring new clinical pathways and treatments.
    • You will contribute to maintaining high standards in clinical care planning…
    • The CSO drives scientific excellence across discovery, development, clinical evidence generation, and regulatory strategy while cultivating a high‑performance…
    • Deep understanding of clinical research service lines (e.g., full-service offer, FSP and RWLP) and the full drug development lifecycle.
    • Experience managing multiple studies or workstreams in parallel, remaining organised and effective in a fast‑paced, live clinical research environment.
    • You will see clinical research happening in real time and understand how new medicines move from development to patients.
    • Extensive clinical research experience within a CRO or biopharmaceutical environment, including at least 4 years of full project management accountability on…
    • Extensive clinical research experience within a CRO or biopharmaceutical environment, including at least 2 years of full project management accountability on…

People also searched:

clinical trial
research assistant
pharmaceutical
clinical trials
clinical trial coordinator
research
part time
clinical research associate
psychology
researcher

Job Post Details

Clinical Research Nurse - job post

Panthera Biopartners
4.0 out of 5 stars
2 Oak Rise, York YO24 4LJ
From £35,000 a year - Full-time

Job details

Pay

  • From £35,000 a year

Job type

  • Full-time

Shift and schedule

  • Monday to Friday

Location

2 Oak Rise, York YO24 4LJ

Benefits

Pulled from the full job description

  • Annual leave
  • Employee discount
  • Sick pay
  • Life insurance
  • Company pension
  • Private medical insurance
  • Cycle to work scheme

Full job description

Clinical Research Nurse - York

We have an exciting opportunity for a dynamic and motivated Research Nurse to join our brand new site in York!

About us

Panthera is an independent Site Management Organisation helping pharmaceutical and contract research organisations find the right patient, for the right trial, at the right time. The Panthera team is run by a world-class team of experts with more than a hundred years of clinical research experience.

We put the patient at the heart of everything we do to ensure the best experience and environment for volunteers and participants. Accelerating clinical breakthrough for our customers, our patients, and for future generations.

Salary & Benefits Package

  • Salary: £35,000 to £42,000
  • 25 days annual leave plus bank holidays increasing with length of service
  • Annual Leave Buy and Sell Scheme
  • Life insurance - 3x annual salary
  • Employee healthcare cash plan
  • Employee Assistant Programme
  • Enhanced sickness and family friendly policies
  • Annual Self Care Day
  • Cycle to Work Scheme
  • EV Scheme

Job Summary

The post holder will be responsible for ensuring that nursing activities, related to clinical trials across a wide and diverse range of therapeutic areas, are undertaken following Nursing and Midwifery Council guidelines and as per Good Clinical Practice (ICH-GCP). You will work alongside the wider clinical research team in the assessment and management of patient care pathways. This will involve recruitment, education, monitoring of research participants and the collection and documentation of accurate data.

As a skilled communicator, the successful candidate, must also possess excellent interpersonal and problem-solving skills and be able to act as an ambassador for promoting research utilisation and best practice.

The normal working hours for the post are Monday to Friday, 8:30am - 4:30pm, although the post holder may need to be flexible to accommodate patient visits and assessments outside of these hours when required.

Key Responsibilities

  • Manage nursing activities relating to clinical trials from the start up on a trial to the close out, working to ICH/GCP guidelines
  • Attend site initiation visits (SIV) for any new study and keep up to date with any changes with the study protocols
  • Perform PIV patient interest visits (chats) effectively with knowledge and understanding of the study protocol
  • Keep patients engaged with the study at each visit to optimize patient retention
  • Collecting records, verifying, and entering study data into the source notes, CRF/eCRF and all associated paperwork with a high degree of accuracy
  • Promoting and nurturing a welcoming, professional and pleasant environment for staff and participants
  • Ensuring that all data queries are acted upon in a timely and efficient manner
  • Initiating any emergency reaction when required at site for patients or staff
  • Review and regularly check the emergency trolley
  • To be able to perform laboratory duties on each study if required
  • Always work in compliance of GDPR (General Data Protection Regulation)
  • To keep up to date with all training, ongoing SOPs/COPs and regulatory standards

Ideal Candidate

  • NMC Registration with no limitations to practic
  • Experience in a fast paced environment
  • 2+ years post registration experience
  • Clinical research experience (desirable)
  • Ability to work in a team within a multidisciplinary environment with minimal supervision
  • A patient focused attitude
  • Self-motivated and excellent organisational skills

Interested? Come and join our journey!

Panthera Biopartners is an equal opportunity employer. Panthera will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. Panthera only employs individuals with the right to work in the country where the role is advertised.

INDHP

Job Type: Full-time

Pay: From £35,000.00 per year

Benefits:

  • Company events
  • Company pension
  • Employee discount
  • Life insurance
  • On-site parking
  • Private medical insurance
  • Sick pay

Work Location: In person

Let Employers Find YouUpload Your Resume