All in with your dermatology & rheumatology clinical development
Montreal, Quebec
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.
Télétravail · Canada
The Project Manager oversees the end-to-end lifecycle of clinical trials, ensuring compliance with budgets, timelines, and regulatory standards. They act as the primary point of contact for sponsors and internal teams while managing operational aspects such as site activation, vendor coordination, and risk mitigation.
Sur place · Montréal
The Patient Recruitment Assistant provides information to patients regarding clinical research studies and verifies their eligibility. Responsibilities include managing patient files, conducting inbound and outbound calls, and scheduling screening appointments.
Télétravail · Canada
The Project Manager II is responsible for the end-to-end management of clinical trials, including planning, execution, monitoring, and closure. They act as the primary contact for sponsors and coordinate cross-functional teams to ensure compliance with budgets, timelines, and regulatory standards.
Télétravail · Canada
The IT Support Services Manager oversees daily Service Desk operations, endpoint management, and vendor relationships to ensure high-quality service delivery. They lead a team of support personnel while driving continuous improvement, automation, and compliance with regulatory standards.
Télétravail · Canada
The Proposal Writer Specialist is responsible for developing scientific and technical content for study proposals and responding to RFIs. They coordinate with internal subject matter experts and external KOLs to ensure accurate, compelling, and compliant proposal delivery.
Sur place · Montréal
The Finance Intern will support daily accounting, financial reporting, and administrative tasks, including accounts payable and receivable. They will assist with reconciliations, month-end closing activities, and the maintenance of accurate financial data within accounting systems.
Télétravail · Canada
Responsible for developing and writing scientific and technical content for study proposals and responding to RFIs. Coordinates with internal subject matter experts and external KOLs to ensure accurate, compelling, and compliant proposal delivery.
Sur place · Montréal
The Patient Recruitment Assistant provides information on clinical research studies and verifies patient eligibility. Responsibilities include managing patient files, conducting inbound and outbound calls, and scheduling screening appointments.
Télétravail · Canada
The Graphic Designer creates high-quality visual communications and assets across digital, print, and multimedia formats to support corporate objectives. This includes transforming complex scientific and medical content into engaging visuals while leveraging AI tools to accelerate production.
Sur place · Montréal
The Quality Systems Specialist maintains a compliant quality system by conducting internal audits and managing CAPAs and deviations. They also handle vendor qualification, support regulatory inspections, and contribute to the writing of quality documentation.
Télétravail · Canada
This role combines people leadership with operational delivery, overseeing regulatory submissions to Ethics Committees and Regulatory Authorities for clinical trials. The manager is responsible for resource management, team development, and ensuring compliance with regional regulatory guidelines.
Télétravail · Canada
Oversee Ethics Committee and Regulatory Authority submissions to ensure compliance with regulations and contractual timelines. Provide line management for direct reports, including resource allocation, mentoring, and professional development.
Hybride · Montréal
Provide high-level administrative and operational support to the CEO, managing communications, calendars, and professional documentation. Coordinate scientific publications, advisory board meetings, and administrative tasks related to the MDRI grant program.
Télétravail · Canada
Oversees the initiation, planning, and execution of early phase and translational clinical trials, ensuring they are audit-ready and within budget. Acts as the primary point of contact for sponsors and vendors while mentoring other project managers.
Télétravail · Canada
Responsible for the operational management and oversight of clinical investigative sites and monitoring deliverables for clinical trials. This includes training CRAs, identifying quality issues, and ensuring timelines and regulatory requirements are met.
Sur place · Montréal
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.
Sur place
The Clinical Scientist is responsible for medical writing activities at Indero. The individual will author or contribute to development of clinical and regulatory documents (synopsis, study protocols, statistical analysis plans, clinical study reports), as well as scientific publications. This role will be perfect for you if: You are a strong medical writer with demonstrated ability to produce high-quality scientific documents to support clinical research. You enjoy learning continuously and keeping yourself informed. Having an impact within a growing company with momentum motivates you. RE…
Télétravail · Canada
The Proposal Writer Specialist is responsible for preparing coherent proposal documents throughout the operational process and supporting the business development team during the pre-contractual phase. This includes responding to RFIs and developing scientific and technical content for study proposals.
Télétravail · Canada
Responsible for developing and validating SDTM and ADaM datasets, as well as Tables, Listings, and Figures (TLFs) for clinical study reports. The role involves collaborating with biostatistical teams to ensure deliverables meet regulatory requirements and company SOPs.
Télétravail · Canada
Responsible for developing and validating SDTM and ADaM datasets, as well as Tables, Listings, and Figures (TLFs) for clinical study reports. Collaborates with biostatistical teams to ensure deliverables meet ICH guidelines and regulatory requirements.