Clinical Trial Nurse Courtice, Ontario

IQVIA; Quebec; On-site; CAD 80,000 - 100,000; Part time

Job summary

Un fournisseur mondial de services de recherche clinique recherche un soutien clinique à temps partiel. Vous devrez coordonner des essais cliniques, recruter des patients et garantir la conformité avec les réglementations. Des compétences en soins aigus et une expérience en administration d'injections sont nécessaires. Le poste est situé à Québec, et vous ferez partie d'une équipe engagée à améliorer la santé des patients.

Qualifications

• Connaissances des systèmes EMR et des pratiques médicales liées.
• Expérience dans un environnement hospitalier et en soins aigus.
• Capacité à administrer des injections et à fournir des soins à domicile.

Responsibilities

• Coordinating and participating in clinical research studies.
• Collecting and submitting regulatory documentation as required.
• Recruiting and screening patients for clinical trials.

Skills

Systèmes EMR

Expérience à l'hôpital

Soins aigus

Expérience en soins intensifs

Injectables dermiques

Expérience dans l'administration d'injections

Soins à domicile

Infirmier

Expérience Botox

Expérience en soins critiques

Administration de médicaments

Alimentation par sonde

Job description

Job Overview : Part time - 24 hours / wk and onsite support.

Coordinate and participate in clinical research studies ensuring that studies are carried out according to

protocol contracted scope of work good clinical practice sponsor standard operating

procedures (SOPs) and any relevant local guidelines and regulations.

Essential Functions

Provides clinical research support to investigators to prepare for and execute assigned research studies

Reviews study protocols source document forms other study-specific documents and electronic data

capture systems used to record clinical research data

Collects and submits regulatory / ethics documentation as required by the Federal Drug Administration

(FDA) and other regulatory bodies governing the conduct of the study

Recruits and screens patients for clinical trials and maintain subject screening and enrollment logs

Orients research subjects to the study including the purpose of the study procedures and protocol

requirements such as timeline for visits

Maintains source documentation based on protocol requirements that adhere to Good Clinical Practice

(GCP) / International Conference on Harmonization (ICH) documentation principles

Schedules and executes study visits and perform study procedures as delegated and supervised by the

Principal Investigator

Handles lab testing and analysis including preparation of specimen collection tubes and lab logistics

Monitors subject safety and report adverse events and reactions to Principal Investigator study team

members and IRBs as appropriate

Corresponds with research subjects to troubleshoot study-related questions or concerns

Participates in routine meetings with site study staff and Investigators to confirm study tasks are assigned

and are executed to the expected standards

Actively involved in study data quality checking and query resolution

Performs a variety of complex clinical research procedures including but not limited to electrocardiogram

(ECG) lab sample collection spirometry vital signs dose verifications cardiac telemetry monitoring and

questionnaire administration

Updates and maintains site staff skills training and knowledge of current best nursing practices and topics

related to clinical research

Assists the investigators to safeguard the well-being of subjects and maintain standards required of

clinical research sites

Maintains a safe environment in accordance with site policies

Acts as an advocate for research subjects

Addresses subject questions in a pro‑active manner and take remedial action as required

Assists and advise site staff in nursing practices and on the delivery of study care to subjects

Reports any deviations from normal research practices to senior staff and implement agreed changes in

the study care program

Assists investigator in verifying that research study objectives are met on time within budget and

according to application protocol requirements clinical research regulations and quality standards

Assists in providing training to new investigator site staff members on study‑specific topics and

requirements

Maintains adherence to investigator site staff training requirements by auditing and maintaining training

records

Provides guidance and supervision to lower level site staff to help provide that processes are carried out

in line with protocols and SOPs where applicable

Participates in study process reviews and enhancement efforts to support control of site unit budget

development of the research facilities and site services and the culture towards a high performing research

study team

Prepares for and attend study monitoring visits study audits and regulatory inspections with clinical

research regulatory agencies

Adheres to standard operating procedures (SOPs) and other directives throughout this process

Assists research site with coverage planning related to staffing and scheduling for research projects

#LI-CES and #LI-DNP #LI-HCP #ONSITE

IQVIA est un fournisseur mondial de premier plan de services de recherche clinique dinformations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé. IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus visitez

IQVIA est fière dêtre un employeur souscrivant au principe de légalité daccès à lemploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race la couleur la religion le sexe lorientation sexuelle lidentité de genre lorigine nationale le handicap lâge létat matrimonial ou tout autre statut protégé par la loi applicable. Des mesures dadaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure dadaptation nous vous encourageons à contacter notre équipe dacquisition de talents au afin quIQVIA puisse soutenir votre participation au processus de recrutement.

Veuillez noter quil est possible que nous utilisons lintelligence artificielle (IA) dans le traitement de votre candidature. Cependant nous utilisons lIA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures et non pas pour remplacer la prise des décisions par les membres de notre équipe.

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability age marital status or any other status protected by applicable law. Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation we encourage you to contact our Talent Acquisition Team at : so that IQVIA can support your participation in the recruitment process.

Please note that we may use artificial intelligence (AI) in the processing of your application. However we only use AI to assist our recruitment team with the screening or assessment of candidacies and not as a substitute for human decision-making.

Key Skills

EMR Systems,Hospital Experience,Acute Care,ICU Experience,Dermal Fillers,Experience Administering Injections,Home Care,Nursing,Botox Experience,Critical Care Experience,Medication Administration,Tube Feeding

Employment Type : Part-Time

Experience : years

Vacancy : 1