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 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
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.
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.
Remote · Canada
The Clinical Data Manager will lead and manage clinical studies, ensuring data is collected, managed, and reported accurately and securely. They are responsible for developing eCRF specifications, conducting database validation, and overseeing data management documentation throughout the study lifecycle.
Remote · Canada, International Falls, Minnesota, United States
This is a general talent pool posting for future career opportunities at Indero. Interested candidates are invited to submit their interest to be considered for upcoming roles.
Remote · Canada
The Clinical Trial Manager II is responsible for the operational management and oversight of clinical investigative sites and monitoring deliverables for early-phase trials. They also manage project timelines, budgets, and resources while ensuring compliance with regulatory standards and study-specific requirements.
On-site · 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.
Hybrid · Montréal
The IT Technician serves as the first point of contact for technical support, resolving incidents and service requests for employees. Responsibilities include endpoint deployment, identity and access management, and ensuring compliance with IT security policies.
Remote · 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.
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.
Remote · 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.
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 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.
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.
