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    • Utilise your skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials and…
    • You will be responsible for the management of a range of external-facing projects, including clinical trials sponsored by pharmaceutical companies.
    • Experience recruiting patients into clinical trials.
    • Create recruitment plans for all upcoming and active clinical trials.
    • Job Types: Full-time, Permanent.
    • MUST HAVE: Experience in clinical trials..
    • Patient Assessments:* Perform clinical and cognitive assessments as required by trial protocols (e.g., MMSE, MoCA,…
    • Create and maintain healthy and creative relationships with clinical trial sites and Principal Investigators, helping to support and influence where required.
    • Substantial experience in clinical research, clinical data management or study coordination.
    • We are looking for someone who combines strong clinical research…
    • Clear and accurate written communication for clinical note-keeping.
    • A background working with people with a disability, in a care setting, in clinical, sports…
    • Minimum of 3-5 years of experience in clinical research or clinical trial management, with a focus on site management or clinical site engagement.
    • You'll assess how an individual's health conditions affect their daily living and ability to work, using your existing clinical knowledge to gather information,…
    • Key requirements: * Experience in patient care - 2+ years minimum * Experience in clinical evaluation, clinical data assessment, and medical statistics -…
    • Strong understanding of clinical trial design and clinical development, ideally including experience supporting late-phase clinical studies.
    • Strong understanding of global clinical development, clinical operations and regulatory processes.
    • Significant clinical research and clinical development…
    • Negotiate directly with assigned sites on all site related contracting items including clinical trial agreements, budgets, payment terms, ancillary agreements…
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    • To have a working understanding of clinical governance.
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    • Nurse, Paramedic, Physio, or Occupational Therapist…
  • View similar jobs with this employer
    • To have a working understanding of clinical governance.
    • Clinical Auditor – Functional Specialist (PIP) team.
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Clinical Research Nurse
26 Linenhall Street, Belfast BT2 8BG
From £40,000 a year
Part-time, Permanent, Full-time

Job details

Here’s how the job details align with your profile.

Pay

From £40,000 a year

Job type

Part-time
Permanent
Full-time

Benefits

Pulled from the full job description
Employee discount
Company pension

Full job description

Post: Clinical Research Nurse

Employer: Ormeau Clinical Trials Ltd

Starting Salary: £40,000 (negotiable based on experience)

Hours: Full-time (37.5 hours per week). Part-time opportunities are available.

The Opportunity:

If you want to expand your nursing career options outside the NHS, then, why not explore a career as our next Clinical Research Nurse, making a direct impact on patient care by contributing to the development of new medical treatments.

This is an outstanding opportunity to join an enthusiastic team of Clinical Research Nurses. The clinical team manage a variety of simple and complex national and global clinical trials. The successful candidates will have professional responsibility to coordinate specific research studies providing care and study related treatment to all participants. The post holder is also expected to act as an associate nurse for other trials within the unit under guidance from the Principal Investigator (PI).

On a normal day, you will:

  • Utilise your skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon nursing standards.
  • Utilise your nursing assessment skills to observe participant general well-being and potential adverse events.
  • Document adverse events and take appropriate action as needed.
  • Educate, explain and inform participants of study procedures.
  • Conduct comprehensive patient assessments and collect detailed medical histories in compliance with Good Clinical Practice (GCP) and the study protocol.
  • Administer investigational product to participants according to the protocol and applicable regulations.
  • Perform study related activities such as vital signs, ECGs, venepuncture, spirometry etc.
  • Collect and process biological samples according to the study protocol and Standard Operating Procedures (SOP).
  • Record data obtained in a timely, error free manner according to the protocol and SOP, transcribing source data onto the Case Report Form (CRF).

Additional Responsibilities (Including But Not Limited):

  • Facilitate Clinical Research Associates (CRA) during monitoring meetings.
  • Assist in facilitating closeout visits as needed for trial completion.
  • Develop protocol-specific study data sheets to ensure consistent procedures and data collection.
  • Monitor and replenish trial study supplies based on study requirements.
  • Safely maintain laboratory equipment, supplies, and specimens.

Your Qualifications/Skills:

  • First level registered nurse with at least 3 years of post registration experience, research experience is preferred but not essential.
  • Educated to degree level.
  • Proficient in Microsoft Office, including Word and Outlook and confident working with database systems.
  • Excellent attention to detail.

Previous Clinical Research Nurse experience is ideal, but not a must. We are open to consider recent graduates.

What do you get?
We offer a competitive salary (higher starting salary compared to NHS Band 5) and a comprehensive benefits package, including:

  • Traditional working hours.
  • Full Figs uniform and Nike trainers.
  • NMC annual subscription.
  • Life Support Training provided: BLS.
  • Death in Service benefit.
  • Pension option.
  • Car parking option.

If you are ready to take your nursing career to the next level and make a difference in clinical research, apply now to join our dynamic team at Ormeau Clinical Trials.

Job Types: Full-time, Part-time, Permanent

Pay: From £40,000.00 per year

Benefits:

  • Company pension
  • Employee discount

Application question(s):

  • Experienced in phlebotomy (required)

Experience:

  • Nursing: 3 years (required)

Licence/Certification:

  • NMC (required)

Work Location: In person

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