Jobs at Innovaderm Research

Manage full-cycle recruiting, including sourcing, screening, interviews, candidate communication, offers, background checks, and onboarding transitions. Partner with hiring managers to define recruitment needs and strategies, maintain applicant tracking systems, support employer branding and social media initiatives, produce recruiting analytics, and lead talent acquisition projects. The role requires bilingual French and English communication, HR knowledge, confidentiality, and familiarity with clinical practices and Health Canada and FDA guidelines.

Leads portfolios of dermatology and rheumatology clinical studies, overseeing Project Managers, budgets, vendors, timelines, quality, regulatory compliance, risk mitigation, client relationships, and proposal development. The role manages multinational Phase III trials and provides therapeutic and operational leadership across study teams.

Coordinates site activation and maintenance activities for clinical trials, including collecting and reviewing regulatory documents, managing site communications, maintaining CTMS and eTMF records, supporting ethics submissions, coordinating training and study logistics, and preparing trackers and reports. The role identifies risks, supports audits and inspections, contributes to process improvements and SOP compliance, and provides guidance to junior coordinators.

Coordinates clinical trial site activation and maintenance across the study lifecycle. Responsibilities include reviewing essential and regulatory documents, managing activation timelines, communicating with sites and study teams, maintaining eTMF and study files, tracking enrollment and supplies, coordinating training and meetings, reconciling payments, preparing reports, and supporting audits, inspections, and CAPA activities. The role may also perform project management duties, mentor junior coordinators, and support process improvement.

The Statistical Programmer develops, maintains, and validates datasets and reports for clinical trials, ensuring high-quality deliverables while adhering to industry standards and guidelines.

Manages clinical research projects from initiation through closeout, coordinating sponsors, vendors, sites, and internal teams. Oversees budgets, timelines, site activation, recruitment, regulatory submissions, essential documents, training, monitoring support, data review, risk management, and study deliverables. Ensures compliance with SOPs, GCP, ICH standards, and applicable FDA and Canadian regulations while supporting quality and inspection readiness.

Oversee portfolios of multinational clinical studies, including project managers, budgets, timelines, vendors, quality, regulatory compliance, risk mitigation, and client relationships. Lead operational proposal development, pricing, business development, performance improvement, and therapeutic-area strategy. Provide mentoring and leadership for project management teams while ensuring adherence to GCP, ICH guidelines, SOPs, and FDA and Health Canada requirements.

Lead planning, execution, monitoring, and closeout of Phase I/II clinical trials. Manage budgets, timelines, vendors, TMF, site activation, regulatory submissions, risk mitigation, stakeholder communications, and CRA oversight to ensure GCP/ICH/FDA and Health Canada compliance.

The Project Manager II is responsible for managing clinical trials, overseeing project resources, ensuring compliance with SOPs, and maintaining communication with stakeholders.

Manage Service Desk and endpoint services, lead support staff, ensure SLA-driven incident resolution, drive automation and continual improvement, enforce compliance (GxP, FDA, ISO 27001), manage vendors, and support infrastructure and security projects to improve user experience and operational readiness.

Support and maintain GxP-compliant quality systems: plan and conduct internal audits, manage CAPAs and deviations, review NCs and quality indicators, support vendor qualification and RFIs, assist with inspection readiness and client audits, create training and quality documentation, and perform IP release with GMP background.