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.
Remote · Canada, United States
The Senior Clinical Operations Manager provides line management and performance oversight for clinical personnel while ensuring high-quality, compliant trial management. They are also responsible for driving innovation, continuous improvement, and the adoption of AI-enabled technologies within the clinical operations department.
Hybrid · Québec
The Specialist supports the design, implementation, and improvement of organizational development, talent management, and employee experience initiatives. They coordinate projects, analyze workforce data, and facilitate learning and change management programs to support organizational goals.
On-site · Montréal
The Patient Recruitment Assistant establishes contact with potential patients to verify their eligibility for clinical research studies. They are also responsible for maintaining patient databases and scheduling screening appointments.
On-site · Montréal
The Patient Recruitment Assistant establishes contact with potential study participants to verify their eligibility for clinical research projects. They are also responsible for maintaining patient files in the database and scheduling screening appointments.
Remote · Canada
The Clinical Trial Delivery Trainer develops, maintains, and delivers training programs for clinical trial staff to ensure operational readiness and regulatory compliance. They also provide coaching, facilitate knowledge sharing, and collaborate with leadership to improve training effectiveness and organizational processes.
Remote · Canada
The Director of Vendor Management leads the enterprise vendor governance program, overseeing vendor qualification, performance, risk, and strategic partnerships. They collaborate cross-functionally to ensure vendor services support clinical trial delivery while managing VMO resources and budgets.
Remote · Canada
The Project Manager oversees the initiation, planning, and execution of clinical research projects while managing study-specific vendors throughout the project lifecycle. They act as the primary contact for sponsors and internal teams to ensure project deliverables meet budget, scope, and regulatory requirements.
Remote · Canada
The senior clinical scientist is responsible for authoring and reviewing clinical and regulatory documents, including study protocols, statistical analysis plans, and clinical study reports. They also provide scientific expertise during study conduct, mentor junior staff, and support business development initiatives.
Remote · Canada
The Legal Specialist supports the Legal Department by managing clinical research contracts, ensuring regulatory compliance, and maintaining legal documentation. They also coordinate contract execution workflows and provide administrative support for privacy assessments and internal legal inquiries.
Remote · Canada
The Project Manager oversees the initiation, planning, and execution of early-phase clinical research projects while managing investigative sites and monitoring deliverables. They ensure compliance with study budgets, timelines, and regulatory requirements while serving as a primary contact for sponsors and internal teams.
Remote · Canada
The Biostatistician will act as a lead or support on phase 1 to 4 clinical trials, overseeing statistical protocols, analysis plans, and data management documentation. They will also manage project budgets, timelines, and collaborate with cross-functional teams to ensure compliance with regulatory standards.
On-site · Toronto
The Senior Talent Acquisition Advisor manages the full-cycle recruitment process and acts as a business partner to hiring managers to identify and attract top talent. They are also responsible for developing sourcing strategies, maintaining recruitment systems, and supporting employer branding initiatives.
On-site · Montréal
The Regulatory Affairs Specialist oversees Ethics Committee and Regulatory Authority submissions to ensure compliance with regulations and contractual timelines. They also provide leadership for clinical trial start-up activities and serve as a point of contact for sponsors and subcontractors.
Remote · 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.
On-site · Montréal
The Financial Project Analyst tracks and reports on project profitability while collaborating with project teams and clients to ensure financial performance. Responsibilities include project budget setup, revenue and expense recognition, invoicing management, and providing financial guidance to project managers.
On-site · Montréal
The Senior Statistical Advisor provides statistical input for clinical trial development, including protocol design, sample size estimation, and data analysis. They also ensure all research activities comply with regulatory requirements and industry standards while collaborating with cross-functional teams.
Remote · 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.
Remote · Canada
The Talent Acquisition Advisor acts as a business partner to hiring managers to manage the full-cycle recruitment process and develop effective sourcing strategies. They are responsible for ensuring a positive candidate experience, maintaining recruitment systems, and supporting employer branding initiatives.
Remote · Canada
The Project Director oversees a portfolio of clinical studies, managing project managers and ensuring adherence to quality standards and regulatory requirements. They also lead operational contributions to business development, proposal pricing, and client satisfaction.
Remote · Canada
The TMF Document Coordinator II manages and performs quality control on clinical trial documentation to ensure compliance with regulatory standards and study-specific guidelines. They also independently lead TMF activities for Investigator-Initiated Studies and smaller sponsored projects, including oversight of the eTMF from start to closeout.
