Clinical Trial Nurse - Courtice, Ontario

IQVIA; Toronto; On-site; CAD 100,000 - 125,000; Part time

Job summary

A global clinical research provider in Toronto is seeking part-time support for clinical research studies. Responsibilities include coordinating studies, recruiting patients, and ensuring compliance with regulatory standards. Ideal candidates will have experience in clinical research and knowledge of Good Clinical Practice. This is an onsite role requiring 24 hours per week.

Qualifications

• Experience in clinical research studies.
• Knowledge of regulatory/ethics documentation requirements.
• Ability to coordinate study procedures.

Responsibilities

• Coordinate and participate in clinical research studies.
• Review and execute study protocols and documents.
• Recruit and screen patients for trials.

Skills

Clinical research support

Patient recruitment

Good Clinical Practice (GCP)

Safety monitoring

Regulatory compliance

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.

Responsibilities

• Provide clinical research support to investigators to prepare for and execute assigned research studies
• Review study protocols, source document forms, other study-specific documents, and electronic data capture systems used to record clinical research data
• Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of the study
• Recruit and screen patients for clinical trials and maintain subject screening and enrollment logs
• Orient research subjects to the study including the purpose of the study, procedures and protocol requirements such as timeline for visits
• Maintain source documentation based on protocol requirements that adhere to Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) documentation principles
• Schedule and execute study visits and perform study procedures as delegated and supervised by the Principal Investigator
• Handle lab testing and analysis including preparation of specimen collection tubes and lab logistics
• Monitor subject safety and report adverse events and reactions to the Principal Investigator, study team members and IRBs as appropriate
• Correspond with research subjects to troubleshoot study-related questions or concerns
• Participate in routine meetings with site study staff and Investigators to confirm study tasks are assigned and executed to the expected standards
• Actively involved in study data quality checking and query resolution
• Perform 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
• Update and maintain site staff skills, training and knowledge of current best nursing practices and topics related to clinical research
• Assist the investigators to safeguard the well-being of subjects and maintain standards required of clinical research sites
• Maintain a safe environment in accordance with site policies
• Act as an advocate for research subjects
• Address subject questions in a pro-active manner and take remedial action as required
• Assist and advise site staff in nursing practices and on the delivery of study care to subjects
• Report any deviations from normal research practices to senior staff and implement agreed changes in the study care program
• Assist investigators in verifying that research study objectives are met on time, within budget and according to application protocol requirements, clinical research regulations and quality standards
• Assist in providing training to new investigator site staff members on study-specific topics and requirements
• Maintain adherence to investigator site staff training requirements by auditing and maintaining training records
• Provide guidance and supervision to lower level site staff to help ensure processes are carried out in line with protocols and SOPs, where applicable
• Participate 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
• Prepare for and attend study monitoring visits, study audits and regulatory inspections with clinical research regulatory agencies
• Adhere to standard operating procedures (SOPs) and other directives throughout this process
• Assist 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, d'informations 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 https://jobs.iqvia.com

IQVIA est fière d’être un employeur souscrivant au principe de l’égalité d’accès à l’emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap, l’âge, l’état matrimonial ou tout autre statut protégé par la loi applicable. Des mesures d’adaptation 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 d’adaptation, nous vous encourageons à contacter notre équipe d’acquisition de talents au [e-mail], afin qu’IQVIA puisse soutenir votre participation au processus de recrutement.

Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA 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 https://jobs.iqvia.com

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: [e-mail], 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.