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Clinical Research Nurse – London – CRO – Up to £42,000 DOE + Benefits

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The Company

  • A leading full service CRO specialising in infectious and respiratory diseases.

  • Due to increasing portfolio of studies and an ever-increasing need for development in this sector space, our client is looking to grow their team.     

The Role

  • To maintain and promote the safety and wellbeing of all subjects participating in a clinical trial within the regulatory frameworks of ICH GCP, other statutory instruments and NMC Code of Conduct.

  • Assist the senior team with the daily management and allocation of workload within the clinical environment

  • Involvement in preparing, planning and execution of daily clinical activities;

  • Provide guidance and mentoring to staff in the clinical environment. Ensure competence in performing their own and team’s daily tasks;

  • Supervision of new ancillary staff in the clinical environment as required;

  • Promote and adhere to Company SOP’s, protocols and Health and Safety Regulations; and

  • Support Clinical Support Specialists in performing clinical assessments as per protocol;

  • Perform nurse specific procedures as identified within the protocol;

  • Performs informed consent procedures as identified in the study protocol;

  • Completion of study related documents e.g. logs, source data and CRFs;

  • Adhere to Company SOPs, protocols and Health and Safety Regulations;

  • Use of expertise to input into the development of SOPS and other procedural documents;

  • Maintain subject safety at all times responding to emergencies as per internal SOP and national guidelines and protocols;

  • Monitoring and identification of the deteriorating subject, with appropriate escalation;

  • Responsible for the checking of emergency resuscitation equipment as per SOP/OIs;

  • Responsible for maintenance of medicines management within the clinical department as per SOP/OI;

  • Responsibility for the supervision of clinical staff in the screening unit as delegated by the Senior Research Nurse;

  • Identification of areas for service improvement;

  • Promotes a high standard of practice and care at all times

You

  • NMC registration essential and Nursing qualification essential

  • 1+ years’ experience working as a clinical research nurse or equivalent.

  • Certificate in basic or intermediate life support essential

  • Sound clinical knowledge

  • Competence in the recording of medical history, vital signs, ECG, phlebotomy etc essential

  • Knowledge of GCP. Previous experience in a clinical trials setting is desirable but not essential

  • Ability to prioritise own workload

  • Ability to manage adverse events or clinical incidents

  • An understanding of ethical practice and confidentiality

  • Good knowledge of ICH-GCP and regulatory standards

What should you do next?

Are you a clinical research nurse looking to take your career to the next level? Wanting to broaden your experience across the industry? This is one to watch!

To discuss this role further or to find out about other roles I’m currently working on, please get in touch or hit apply to submit your current CV.

Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.

Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.

If there are any arrangements or adjustments, we can make to assist you at interview then please let us know and we'll be more than happy to assist.

 

Apply Now!

Job Consultant

Matteo Berogna

Clinical Research

Recruitment Consultant

+44 (0) 2394 214 480

matteo@carrotpharma.co.uk

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