Strategist, Patient Recruitment & Site engagement / Stratégiste, Recrutement de patients
Montreal, Quebec, Canada · On-site
Mid level
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Project Manager II / Gestionnaire de projet II (Canada)
Montreal, Quebec, Canada · Remote OK
Senior
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Spécialiste, rédaction de propositions/Proposal Writer Specialist
Montreal, Quebec, Canada · Remote OK
Mid level
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Full-time
high school, bachelor degree
Medical Insurance, Dental Insurance, Vision Insurance, RRSP, Vacation, Personal Days
Posted 2d ago
~40 hrs/week
Responsibilities
Develop and implement project and site-level patient recruitment strategies while monitoring enrollment progress to ensure targets are met. Collaborate with project managers and clients to design advertisement materials and coordinate IRB approvals.
Requirements
Requires a Bachelor's degree in Communications or a related field with 3 years of experience, or a high school diploma with 5 years of experience. Must have at least 2 years of relevant experience in the biotechnology, pharmaceutical, or CRO industry.
Full job description
The Strategist, Patient Recruitment & Site engagement works with the Associate Director, Patient recruitment strategies and Development and the Specialist, Multimedia & Recruitment in supporting patient recruitment strategies and site engagement.
This role will be perfect for you if:
Have at least 2 years’ experience in patient recruitment strategies & Site engagement
Have experience working with Patient Advocacy groups
Have strong organizational and communication skills
More specifically, the Strategist, Patient Recruitment and Site Engagement must:
Develops the project level and site level recruitment strategy plan in collaboration with the Patient Recruitment Team.
Informs and trains project team on recruitment strategy in collaboration with the Project Manager and/or CTM
Participates in BD handover, Kick off Meeting, Investigator meeting
Develops the sites recruitment plan study template and ensure customization of this plan with each site.
Monitors the progression of subject enrolment to ensure the target can be achieved and proposes improvements in recruitment strategies, as necessary, in collaboration with the Project Manager/CTM and/or clinical team
Collaborates with Strategist, Patient Recruitment to create recruitment models based on information obtained during feasibility, site initiation, actual recruitment performance.
Collaborates with Strategist, Patient Recruitment to create the enrolment tracker with recruitment projections using CTMS or other system/tracker
Works with SSU and project manager to obtain updated recruitment projections from sites post activation to forecast LPI or propose new strategies for recruitment which may include increasing sites, adding additional advertisement initiatives, physician outreach, etc.
Assists the Project Manager on client’s request for recruitment and advertisement.
Interacts directly with client to establish and gain client input on recruitment strategies and budgets.
Creates and designs image and script advertisements for studies, in respect of Media’s and appropriate ethics committee’s current guidelines
When applicable, offers guidance to sites on ways to achieve their recruitment target using their advertisement budget
Ensures that all project relevant documentation is sent for filing in eTMF and archiving
Coordinate global advertisement IRB submission and approval process
Requirements
IDEAL PROFILE
Education
BA/BS required, preferably in Communications or related field with 3 years relevant experience OR a high school diploma / DEC with 5 years relevant experience
Experience
Minimum of 2 years of relevant work experience in the biotechnology, pharmaceutical or CRO industry
Knowledge and skills
Knowledge of good clinical practice, ICH standards and applicable regulations
English spoken and written, Spanish or French an asset
Experience in a research site environment an asset
Experience managing Patient advocacy group an asset
Experience in Patient recruitment strategies an asset
Problem solving skills, good adaptability, versatile, and great attention to details
Strong organizational, communication, problem-solving and multi-tasking skills
Problem solving skills, and great attention to details
Strong organizational, communication, and multi-tasking skills
Our company
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 opportunities for advancement.
In this position, you will be eligible for the following perks:
Flexible work schedule
Permanent full-time position
Comprehensive benefits (medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, social activities)
Ongoing learning and development opportunities
About Indero
Indero is a contract research organization (CRO) specialized in clinical trials. Based in Montreal, we have built a strong reputation for the quality of our research and services that exceed client expectations. Indero continues to grow and expand across North America and Europe.
Indero is committed to providing equitable treatment and equal opportunity to all individuals. Accommodations are available throughout the recruitment and selection process for applicants with disabilities, upon request.
Please note that Indero only accepts applicants who are legally authorized to work in Canada.
Description de poste
Le Stratégiste, Recrutement de patients et engagement des sites, travaille avec le Directeur Associé, Stratégies de recrutement de patients et Développement et le Spécialiste, Multimédia et Recrutement, pour soutenir les stratégies de recrutement de patients et l'engagement des sites.
Ce rôle sera parfait pour vous si :
Avez au moins 2 ans d'expérience dans les stratégies de recrutement des patients et l'engagement des sites.
Avez de l’expérience de travail avec des groupes de patients
Possèder de solides compétences en matière d'organisation et de communication
Plus précisément, le stratège, recrutement de patients et engagement des sites doit :
Élaborer le plan de stratégie de recrutement au niveau du projet et du site en collaboration avec l'équipe de recrutement de patients.
Informe et forme l'équipe de projet sur la stratégie de recrutement en collaboration avec le chef de projet et/ou le CTM.
Participer à la remise des BD, aux réunions de lancement, aux réunions des investigateurs.
Développe le modèle d'étude du plan de recrutement des sites et assure la personnalisation de ce plan avec chaque site.
Surveille la progression du recrutement des sujets pour s'assurer que l'objectif peut être atteint et proposer des améliorations aux stratégies de recrutement, si nécessaire, en collaboration avec le chef de projet/CTM et/ou l'équipe clinique.
Collaborer avec le stratège, recrutement de patients, pour créer des modèles de recrutement basés sur les informations obtenues pendant la faisabilité, le lancement du site, les performances réelles de recrutement.
Collaborer avec le stratège, recrutement de patients, pour créer le suivi des inscriptions avec des projections de recrutement en utilisant le CTMS ou un autre.
Travailler avec l'USS et le chef de projet pour obtenir des prévisions de recrutement des sites, après l'activation afin de prévoir l'IPV ou de proposer de nouvelles stratégies de recrutement qui peuvent inclure l'augmentation du nombre de sites, l'ajout d'initiatives publicitaires supplémentaires, la sensibilisation des médecins, etc.
Aider le gestionnaire de projet à répondre aux demandes de recrutement et de publicité du client.
Interagir directement avec le client pour établir et obtenir son avis sur les stratégies et les budgets de recrutement.
Créer et concevoir des images et des scénarios publicitaires pour les études, dans le respect des directives actuelles des médias et du comité d'éthique approprié.
Donner des conseils aux sites sur les moyens d'atteindre leur objectif de recrutement en utilisant leur budget publicitaire.
S'assurer que toute la documentation relative au projet est envoyée pour être classée dans eTMF et archivée.
Coordonner le processus de soumission et d'approbation de l'annonce globale à l'IRB.
Profil recherché
PROFIL IDEAL
Éducation
BA / BS requis, de préférence en communication ou dans un domaine connexe
Expérience
Minimum de deux ans d’expérience pertinente dans un contexte de biotechnologie, de pharmaceutiques ou dans un environnement CRO
Aptitudes et connaissances
Connaissance des bonnes pratiques cliniques, des normes ICH et des réglementations applicables.
Anglais parlé et écrit, espagnol ou français un atout
Expérience dans un environnement de site de recherche, un atout
Expérience de la gestion d'un groupe de défense des patients, un atout
Expérience dans les stratégies de recrutement de patients, un atout
Aptitude à résoudre les problèmes, bonne capacité d'adaptation, polyvalence et grande attention aux détails.
Solides compétences en matière d'organisation, de communication, de résolution de problèmes et de gestion multitâches.
Aptitude à résoudre les problèmes et grande attention aux détails.
Solides compétences en matière d'organisation, de communication et de multitâche.
Notre entreprise
Chez Indero, vous travaillerez avec des collègues compétents et dynamiques. Nos valeurs sont la collaboration, l’innovation, la fiabilité et la réactivité. Nous offrons un environnement de travail stimulant ainsi que de belles perspectives d’évolution professionnelle.
Dans ce poste, vous bénéficierez des conditions suivantes :
Horaire de travail flexible
Poste permanent à temps plein
Gamme complète d’avantages sociaux (assurances médicales, dentaires, 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’Indero
Indero est une entreprise de recherche clinique contractuelle (CRO) spécialisée dans les essais cliniques. Depuis ses débuts, notre entreprise à taille humaine s’est forgé une solide réputation pour la qualité de ses recherches et de ses services, surpassant les attentes de nos clients. Basée à Montréal, Indero poursuit sa croissance à travers l’Amérique du Nord et l’Europe.
Indero s’engage à offrir un traitement équitable et des chances égales à tous les candidats. Des accommodements peuvent être offerts à toute étape du processus de recrutement pour les personnes en situation de handicap, sur demande.
Indero n’accepte que les candidatures de personnes légalement autorisées à travailler au Canada.
Le genre masculin est utilisé sans discrimination, dans le seul but d’alléger le texte.
All in with your dermatology & rheumatology clinical development
Industry
Research Services
Company size
201-500 employees
Founded
2000
Headquarters
Montreal, Quebec
LinkedIn followers
33,826
Indero: Your Dual-Focus CRO for Dermatology & Rheumatology
At Indero, we specialize in providing comprehensive Contract Research Organization (CRO) services for dermatology and rheumatology. Our team feels like an extension of your own, offering scientific guidance, accurate results, and exceptional customer satisfaction.
Our Expertise: With over 25 years of deep medical and operational expertise in dermatology, we seamlessly translate our knowledge to rheumatology. We understand that dermatology and rheumatology are inextricably linked, as immune-mediated inflammatory skin and joint diseases often require similar treatments.
Our Services: We set the standard with our value-added services, including:
• Study Design and Protocol Development
• Regulatory Submissions and Consulting
• Trial Master Files Management
• Project Management
• Investigator/Site Selection
• Patient Recruitment
• Clinical and Medical Monitoring
• Pharmacovigilance
• Data Management and Biostatistical Analysis
• Clinical Study Reports and Medical Writing
Since 2000, Indero has built a strong reputation for the quality of our research and the care we offer to study participants, clients, and sites. We often exceed our clients' timeline expectations, ensuring successful outcomes for every project.
Offices: 3530 Boulevard St-Laurent, Suite 300, Montreal, Quebec H2X 2V1, CA
DermatologyPhase I to IV clinical trialsClinical Research SiteClinical ResearchFull service CRORheumatologyRegulatory Consultingand BiometricsProduct ResearchMedical
All in with your dermatology & rheumatology clinical development
Industry
Research Services
Company size
201-500 employees
Founded
2000
Headquarters
Montreal, Quebec
LinkedIn followers
33,826
Indero: Your Dual-Focus CRO for Dermatology & Rheumatology
At Indero, we specialize in providing comprehensive Contract Research Organization (CRO) services for dermatology and rheumatology. Our team feels like an extension of your own, offering scientific guidance, accurate results, and exceptional customer satisfaction.
Our Expertise: With over 25 years of deep medical and operational expertise in dermatology, we seamlessly translate our knowledge to rheumatology. We understand that dermatology and rheumatology are inextricably linked, as immune-mediated inflammatory skin and joint diseases often require similar treatments.
Our Services: We set the standard with our value-added services, including:
• Study Design and Protocol Development
• Regulatory Submissions and Consulting
• Trial Master Files Management
• Project Management
• Investigator/Site Selection
• Patient Recruitment
• Clinical and Medical Monitoring
• Pharmacovigilance
• Data Management and Biostatistical Analysis
• Clinical Study Reports and Medical Writing
Since 2000, Indero has built a strong reputation for the quality of our research and the care we offer to study participants, clients, and sites. We often exceed our clients' timeline expectations, ensuring successful outcomes for every project.
Offices: 3530 Boulevard St-Laurent, Suite 300, Montreal, Quebec H2X 2V1, CA
DermatologyPhase I to IV clinical trialsClinical Research SiteClinical ResearchFull service CRORheumatologyRegulatory Consultingand BiometricsProduct ResearchMedical