Clinical Trial Manager II, Dermatology & Rheumatology, Gestionnaire d'essais cliniques II, Canada

Indero; Montreal; Hybrid; CAD 80,000 - 120,000; Full time

Job summary

A contract research organization is looking for a Clinical Trial Manager II in Montreal. This role involves overseeing clinical monitoring, managing quality deliverables, and ensuring compliance with regulations. The ideal candidate should have a B.Sc. and extensive experience in clinical trials and CROs, with strong leadership and communication skills. Flexible work arrangements are available.

Benefits

Flexible work schedule

Complete benefits package

Ongoing learning and development

Qualifications

• At least 8 years of experience in clinical research including prior CRA monitoring experience.
• 2+ years experience in a Lead CRA or clinical team lead role.

Responsibilities

• Manage the operational aspects of clinical trials.
• Oversee CRA training and address quality issues.
• Conduct quality control site visits and meetings.

Skills

Strong knowledge of ICH/GCP standards

Excellent communication skills

Leadership and organizational skills

Ability to multitask

Problem-solving ability

Experience in CRO

Education

B.Sc. in a relevant clinical research field

Tools

Microsoft Office Suite

Job description

Overview

Clinical Trial Manager II (CTM II), Dermatology & Rheumatology, Canada

The Clinical Trial Manager II (CTM II), Dermatology & Rheumatology 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 is a therapeutic area 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 Indero, 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.

In this position, you will be eligible for the following perks :

• Flexible work schedule
• Full-time contract position
• Complete benefits (medical, dental, vision, vacation, personal days, virtual medical clinic, social activities)
• Ongoing learning and development

Work location

The successful candidate for this position is given the option to work from home anywhere in Canada, or from our headquarters in Montreal (in accordance with company policies and public health directives).

Occasional visits to our Montreal headquarters may be required or encouraged.

About Indero

Indero is a contract research organization (CRO) specialized in dermatology and rheumatology. 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, Indero continues to grow and expand in North America and Europe.

Indero 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.

Innovaderm only accepts applicants who can legally work in Canada.

Profil recherche: PROFIL RECHERCHÉ

Éducation

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

Expérience

• Au moins 8 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 :

L’environnement de travail

Chez Indero, 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.

Vous bénéficierez des conditions suivantes :

• Flexibilité sur l’horaire
• Poste permanent temps plein
• Gamme d’avantages sociaux (REER, assurances médicales, dentaire, vision, vacances, journées personnelles, clinique médicale virtuelle, rabais sur le transport en commun, activités sociales)
• Bureau à proximité du transport en commun (métro Saint-Laurent ou métro Sherbrooke)
• Travail de la maison ou hybride; au choix
• Formation et développement continus

À propos d'Indero

Indero est une entreprise de recherche clinique contractuelle (CRO) spécialisée en dermatologie et rhumatologie. 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, Indero continue aujourd’hui sa croissance en Amérique du Nord et en Europe.

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

Indero 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.