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
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.
On-site · 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.
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.
Hybrid · Montréal
The Site Selection Specialist acts as the primary contact for site identification and feasibility activities within clinical research projects. They manage investigator relationships, coordinate site qualification visits, and track activities within the Clinical Trial Management System.
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 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.
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.
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, ensuring compliance with budgets, timelines, and regulatory requirements.
Remote · Canada
The Project Coordinator II leads site activation activities and manages essential regulatory and clinical trial documentation. They act as the primary point of contact for investigator sites and ensure compliance with study timelines and quality standards.
Remote · Canada
The Senior Project Coordinator provides administrative and coordinating support for site activation activities and ensures that clinical trial deliverables meet internal and external expectations. They manage site start-up timelines, review essential regulatory documents, and act as a primary point of contact for clinical sites.
Remote · Canada
The Project Manager oversees the initiation, planning, execution, and closure of clinical research projects while ensuring compliance with budgets, timelines, and regulatory standards. They coordinate tasks between departments, manage stakeholder expectations, and supervise site activation activities.
Remote · 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.
Remote · East Riding of Yorkshire, England, United Kingdom
Oversees a portfolio of clinical studies and manages Project Managers to ensure operational delivery and client satisfaction. Leads operational contributions to business development and ensures compliance with regulatory standards and quality guidelines.
