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Clinical Research Nurse - Part time (24 hrs) until end Dec 2020

ICON Public Limited Corporation

Part- time (24 hours per week) Fixed Term Contract until end December 2020 Clinical Research Nurse 1 or 2, dependant on experience Location: Madrid...

Part- time (24 hours per week) Fixed Term Contract until end December 2020

Clinical Research Nurse 1 or 2, dependant on experience

Location: Madrid, Spain

Medinova is a rapidly expanding and dynamic fast track company dedicated to the recruitment and running of clinical trials at its own Research Centres.

We concentrate on quick patient recruitment, high data standards and delivering excellent patient experience resulting in a high level of patient retention. These qualities are what our Sponsors look for in a leading Dedicated Clinical Research Organisation and you can be part of our success story.

This is a great opportunity for a nurse with a keen interest in clinical trials to play an important role in the advancement of new treatments.

Role Responsibility

As a Research Nurse 1 or 2 you are required to participate in the creation and maintenance of a high-quality clinical research environment.

You will initiate and manage nursing activities related to clinical trials, from initiation to termination, per ICH/GCP guidelines and to ensure the commercial success of the centre by recruiting and maintaining optimum patient numbers.

Key Accountabilities:Complete all relevant clinical competency training assessments, and attend all relevant research study protocol training, and complete all mandatory training, per the COP's/SOP's.Perform all visits, observations, safety reporting and interventions with the participants in accordance with procedures and schedule of the study protocol, company SOP's and policies.Stay abreast of all relevant SOPs and regulatory guidance, performing all activities in compliance to these.Carry out PIVs efficiently and effectively to optimise patient recruitment.Encourage patients to continue within the study, and to participate in future trials.Collect, record, verify and enter study data into the source notes, CRF/eCRF, and all associated paperwork, with a high degree of accuracy.Ensure that all data queries are acted upon in a timely and efficient manner.Participates in site and investigator meetings when required.Initiates emergency action when required e.g. cardiac arrest, anaphylaxis management, fire, or critical incidents.

The Ideal Candidate

As a successful Research Nurse 1, you will likely have:Registration with no limitations to practice within NursingPhlebotomy, spirometry and ECG experienceBroad post-registration experienceSome understanding of clinical researchWell-developed interpersonal and communication skillsRelevant clinical skillsStrong motivation and an enthusiastic disposition

A successful applicant for the level 2 position will need previous experience working as a Research Nurse in a controlled medical testing environment.

Package Description

MeDiNova has a great team of professional, smart and energetic people. We focus on continued professional development, engaging and supporting the team within in order to reach the common goals of the business.

About the Company

MeDiNova is a rapidly growing multi-national involved in the clinical trial space with 105 quality research centres across eight countries and three continents. We aim to be the patients' choice for clinical research. Our team of highly trained and dedicated staff live the MeDiNova values of patient engagement, integrity, empowerment, customer service and expertise. MeDiNova is consistently growing, if you would like to find out more about this success story in the making, please visit us at www.medinovaresearch.com

Job posted: 2020-08-02

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