Clinical trial manager Jobs in Montreal, QC

Last updated: 23 hours ago

Clinical Trial Manager II (CTM II) / Gestionnaire d’essais cliniques II- Canada

Innovaderm ResearchMontreal, Quebec, CA

Remote

Permanent

Clinical Trial Manager II (CTM II),.The Clinical Trial Manager II (CTM) is responsible for the operational management and oversight of the clinical investigative sites as well as the clinical monit...Show moreLast updated: 30+ days ago

Lead Clinical Account Manager

DexcomRemote Quebec

CA$86.00 hourly

Remote

Full-time

Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM).Dexcom began as a small company with a big dream : To forever change how diabetes is managed.To...Show moreLast updated: 30+ days ago

Promoted

Clinical Veterinarian

Charles River LaboratoriesLaval, QC, Canada

Full-time +1

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant i...Show moreLast updated: 23 hours ago

Clinical Veterinarian

Charles River Laboratories, Inc.Laval, Queb, CA

Full-time +1

Promoted

LifeFlight Clinical Supervisor - Full Time.

MedavieMontréal, QC, Canada

Full-time

EMC) is a wholly owned subsidiary of Medavie Health Services (MHS) that manages and operates ground ambulance, air medical transport and the medical communications operations in Nova Scotia through...Show moreLast updated: 23 hours ago

Specialist I, Clinical Solutions - SCI

SysmexQC, CA

CA$70,200.00 yearly

This is the time to let your talent come to life.To maximize your knowledge and use it for the greater good.To work with the best professionals using state-of-the-art technology, and improve lives ...Show moreLast updated: 30+ days ago

Promoted

Canadian resident or citizen mothers helper needed

Care.comMontreal, Quebec

Full-time

Hello and welcome to our page : ).My due date : February 11th 2025.Week trial before any contract signed.To be a Canadian resident or citizen with a passport willing to travel with us.Be comfortable ...Show moreLast updated: 19 days ago

Promoted

Clinical Nurse

Bien Chez SoiBrossard, QC

CA$57.03–CA$60.70 hourly

Quick Apply

Description du poste Infirmier(ère).PLACEMENT SOINS SANTÉ ( filiale de BIEN CHEZ SOI).Planifier et évaluer les soins à donner. Eacute;valuer la condition physique et ment...Show moreLast updated: 30+ days ago

Field Clinical Specialist THV

Edwards LifesciencesCanada, Montreal,

CA$70.81 hourly

Full-time

Develops clinical education materials in connection with clinical investigations.Provides expertise and clinical insights on the device, procedure and protocol throughout the life cycle of the clin...Show moreLast updated: 30+ days ago

Data Analyst - Immunology

CellCartaMontreal, QC, CA

Temporary

Quick Apply

Clinical Data Analyst - Immunology Are you looking for an exciting career opportunity in biotech? At CellCarta, our Data Analysts play a pivotal role in advancing drug development by delivering hig...Show moreLast updated: 29 days ago

Clinical Trial Leader (CTL)

ScimegaLaval, Quebec

CA$139,500.00–CA$189,500.00 yearly

Under the direction of the Director, Clinical and Scientific Affairs, the CTL is responsible for execution of clinical trials, from the site selection, start-up and enrollment phases up to the stud...Show moreLast updated: 30+ days ago

Gestionnaire, d’études cliniques / Manager, Clinical Trial

Bristol Myers SquibbCA,QC,Montreal

CA$109,993.00 yearly

Full-time

Those aren’t words that are usually associated with a job.But working at Bristol Myers Squibb is anything but usual.Here, uniquely interesting work happens every day, in every department.From optim...Show moreLast updated: 30+ days ago

Site Monitor II- FSP

ParexelRemote, Quebec, Canada

Remote

Full-time

When our values align, there's no limit to what we can achieve.Bilingual- English / French proficiency.The Site Monitor will be responsible for data integrity, data quality and ensuring compliance wi...Show moreLast updated: 30+ days ago

Site Contracts Template Specialist, Clinical Development

PfizerMontreal,Quebec,Canada

CA$23.00 hourly

Remote

Full-time

Must have experience within Biopharmaceutical Industry.The site contracts template specialist is responsible for identifying, prioritizing opportunities, and achieving and maintaining appropriate i...Show moreLast updated: 30+ days ago

Senior Clinical Project Manager.

PSIGreater Montreal Area, QUEBEC, CA

CA$38.79–CA$48.48 hourly

Management of medium-sized (5-15 countries and / or full service) or large (> .Adherence to and promotion of principles of delivery and service in dealing with PSI customers.Project Supervision of sma...Show moreLast updated: 30+ days ago

Associé de recherche clinique, – francophone (Canada), IQVIA Clinical Research Associate - French speaking (Canada), IQVIA

IQVIAMontreal, Quebec, Canada

CA$47,320.00–CA$87,887.80 yearly

Full-time

Participates in the preparation and execution of Phase I to IV clinical trials.Oversees the progress of clinical investigations by conducting interim site assessment, initiation, and closure visits...Show moreLast updated: 30+ days ago

Clinical Trial Manager II (CTM II) / Gestionnaire d’essais cliniques II- Canada

Innovaderm ResearchMontreal, Quebec, CA

30+ days ago

Job type

Permanent

Remote

Job description

Clinical Trial Manager II (CTM II), Canada - North America

The Clinical Trial Manager II (CTM) is responsible for the operational management and oversight of the clinical investigative sites as well as the clinical monitoring deliverables of clinical trials. This includes but is not limited to clinical research associate (CRA) training, identification of quality issues related to site performance and clinical monitoring activities, establishing action plans to address any concerns, as well as ensuring timelines are met.

This role will be perfect for you if :

You enjoy working with a Canadian-owned mid-sized CRO where you can build professional relationships with your colleagues at all levels
You bring previous experience in managing the clinical monitoring portion of clinical projects
Dermatology and rheumatology are therapeutic areas you enjoy or want to learn more about

RESPONSIBILITIES

Ensures that clinical monitoring activities are performed to the Sponsor’s satisfaction, ensuring timely quality deliverables and in accordance with applicable standard operating procedures (SOPs), regulations, good clinical practices and study-specific requirements;

Identifies quality issues and trends related to site performance and clinical monitoring activities through project meetings, site communications, site visit reports and follow-up letters, quality control visits, and quality assurance audit findings. Summarizes findings and establishes action plans to bring corrective actions;

Serves as a point of contact for CRAs and Lead CRAs for assigned projects;

Provides mentoring / oversight of CRAs and Lead CRAs;

Performs site visit report review for assigned projects and tracks site visit report metrics to ensure compliance;

Contributes to the development of the Clinical Monitoring Plan;

Prepares and conducts project-specific training for the CRAs;

Develops the annotated site visit reports and monitoring tools such as source data verification worksheets;

Conducts quality control visits with CRAs;

Coordinates and leads CRA meetings;

Performs co-monitoring visits with CRAs;

May be involved in business development activities (client meetings, proposal defense meetings, requests for proposals (RFPs) requests for information (RFIs)).

Our company : The work environment

At Innovaderm, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.

As a Clinical Trial Manager, you will be eligible for the following perks :

Flexible work schedule

Permanent full-time position

Complete benefits (medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, social activities)

Ongoing learning and development

About Innovaderm

Innovaderm is a contract research organization (CRO) specialized in dermatology with a team of over 175 employees. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Innovaderm continues to grow and expand in North America.

Innovaderm is committed to providing equitable treatment and equal opportunity to all individuals. As such, Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.

We thank you for your application and please note that only those selected for an interview will be contacted.

Description - Fr :

Gestionnaire d’essais cliniques II- Canada

Le Gestionnaire d'essais cliniques II est responsable de la gestion opérationnelle et de la supervision des sites d'investigation clinique ainsi que des livrables de suivi clinique des essais cliniques. Cela comprend, mais sans s'y limiter, la formation des associés de recherche clinique (CRA), l'identification des problèmes de qualité liés à la performance du site et les activités de surveillance clinique, l'établissement de plans d'action pour répondre à toute préoccupation, ainsi que le respect des délais.

Ce poste sera parfait pour vous si :

Vous aimez travailler avec un CRO de taille moyenne de propriété canadienne où vous pouvez établir des relations professionnelles avec vos collègues à tous les niveaux

Vous apportez une expérience antérieure dans la gestion de la partie suivi clinique (monitoring) des projets cliniques

La dermatologie et la rhumatologie sont des domaines thérapeutiques que vous appréciez ou sur lesquels vous souhaitez en savoir plus

RESPONSABILITÉS

S'assure que les activités de surveillance clinique sont effectuées à la satisfaction du commanditaire, en garantissant des livrables de qualité en temps opportun et conformément aux procédures opérationnelles standard (SOP) applicables, aux règlements, aux bonnes pratiques cliniques et aux exigences spécifiques à l'étude;

Identifie les problèmes de qualité et les tendances liés à la performance du site et aux activités de surveillance clinique au moyen de réunions de projet, de communications sur le site, de rapports de visite de site et de lettres de suivi, de visites de contrôle de la qualité et de conclusions d'audit d'assurance qualité. Résume les constatations et établit des plans d'action pour apporter des actions correctives;

Sert de point de contact pour les CRA et les CRA sénior pour les projets assignés;

Assure le mentorat / la supervision des CRA et des CRA sénior;

Effectue la vérification des rapports de visite de site pour les projets assignés et suit les indicateurs de rapports de visite de site pour assurer la conformité;

Contribue à l'élaboration du plan de surveillance clinique;

Prépare et anime une formation spécifique au projet pour les CRA;

Élabore les rapports de visite de site annotés et les outils de suivi tels que les feuilles de travail de vérification des données sources;

Effectue des visites de contrôle de la qualité avec les CRA

Coordonne et dirige les réunions avec les CRA

Effectue des visites de co-monitoring avec les CRA

Peut être impliqué dans des activités de développement des affaires (réunions clients, réunions de défense de proposition, demandes de propositions (RFP), demandes d'informations (RFI)).

Profil recherché : PROFIL RECHERCHÉ

Éducation

B.Sc. dans un domaine pertinent à la recherche clinique, diplôme en sciences infirmières et / ou expérience équivalente;

Expérience

Au moins 5 ans d'expérience en recherche clinique, y compris une expérience préalable en monitoring (CRA) et au moins 2 ans d'expérience dans un rôle de « Lead CRA » ou de chef d'équipe clinique dans l'industrie de la biotechnologie, de la pharmacie et / ou des organismes de recherche sous contrat (CRO);

Aptitudes et connaissances

Solide connaissance des normes ICH / GCP et des exigences réglementaires applicables;

Excellente maîtrise de la suite Microsoft Office (Word, Excel, Power Point);

Capacité à travailler dans un environnement en évolution rapide et à établir de bonnes relations avec les collègues, les sites et les sponsors;

Excellentes compétences en leadership, en organisation, en gestion du temps et en multitâche;

Excellente capacité de jugement et de résolution de problèmes;

Voyage occasionnel (jusqu'à 10% du temps), y compris certains voyages à l'extérieur du pays lorsque possible;

Maîtrise de l'anglais (excellent oral et écrit), le français est un atout;

Expérience en CRO et en dermatologie un atout.

Notre entreprise : NOTRE ENTREPRISE

L’environnement de travail

Chez Innovaderm, vous travaillerez avec des collaborateurs compétents et dynamiques. Nos valeurs sont la collaboration, l’innovation, la fiabilité et la réactivité. Nous offrons un environnement de travail stimulant et des possibilités d’avancement intéressantes.

Dans le poste de Gestionnaire d’essais cliniques, vous bénéficierez des conditions suivantes :

Flexibilité sur l'horaire

Poste permanent à temps plein

Gamme d’avantages sociaux (assurances médicales, dentaire, vision, régime de retraite, vacances, journées personnelles, clinique médicale virtuelle, rabais sur le transport en commun, activités sociales)

Formation et développement continu

À propos d’Innovaderm

Innovaderm est une entreprise de recherche clinique contractuelle (CRO) spécialisée en dermatologie. Depuis ses débuts en 2000, notre entreprise à taille humaine bénéficie d’une solide réputation autant pour la qualité de la recherche effectuée que pour la qualité des soins offerts, dépassant les attentes de ses clients. Basé à Montréal, Innovaderm continue aujourd’hui sa croissance en Amérique du Nord et en Europe.

Innovaderm s’engage à assurer une approche équitable ainsi que des opportunités équivalentes pour tous les candidats. À ce titre, Innovaderm fournira sur demande des accommodations aux candidats ayant un handicap, et ce, à travers toutes les étapes du processus de recrutement, si demandé.

Innovaderm accepte uniquement les candidats pouvant légalement travailler au Canada.

Le genre masculin est utilisé sans discrimination et dans le seul but d'alléger le texte.

IDEAL PROFILE

Education

B.Sc. in a field relevant to clinical research, nursing degree and / or equivalent experience;

Experience

At least 5 years of clinical research experience including prior monitoring experience and at least 2 years of experience acting in a Lead CRA or Clinical Team Leader role in the biotechnology, pharmaceutical, and / or contract research organization (CRO) industry;

Knowledge and skills

Strong knowledge of ICH / GCP standards and applicable regulatory requirements;

Excellent mastery of Microsoft Office suite (Word, Excel, Power Point);

Ability to work in a fast-paced evolving environment and establish good relationships with colleagues, sites and sponsors;

Excellent leadership, organizational, time management and multi-tasking skills;

Excellent judgement and problem-solving skills;

Occasional travel (up to 10% of the time), including some travel outside of the country once possible;

Fluent in English (excellent oral and written), French is an asset;

Experience in a CRO and in dermatology an asset.