Jobs at Innovaderm Research

Supports the Legal Department with clinical research contracts, contract execution, legal documentation, privacy assessments, regulatory compliance, audits, and corporate governance activities. Maintains contract databases and document systems, conducts legal and regulatory research, develops legal templates and SOPs, and coordinates with internal stakeholders, external counsel, notaries, and regulators. The role requires strong organizational skills, confidentiality, contract administration expertise, and familiarity with clinical research, GCP, and privacy regulations.

Supports and leads biostatistical activities across Phase 1–4 clinical trials, including protocol design, sample size calculations, risk-based monitoring, data management, SAPs, TLF shells, CDISC dataset and output review, clinical study reports, and statistical programming teams. Manages deliverable timelines, budgets, forecasting, and quality standards while collaborating with sponsors, vendors, project teams, and regulatory stakeholders. May also support unblinded analyses, randomization, interim analyses, and internal research projects.

Provides statistical expertise across Phase I–IV clinical trials, including protocol design, sample size and power calculations, randomization, statistical analysis plans, data interpretation, clinical study reports, regulatory submissions, SOPs, and client communication. Collaborates with clinical trial teams, supports research and development, and ensures work meets regulatory, industry, sponsor, and timeline requirements.

Maintains Trial Master Files throughout clinical studies by reviewing, classifying, and quality-checking records, resolving queries, tracking milestones and expected documents, preparing metrics and reports, and coordinating TMF reviews and closeout. Independently leads TMF activities for limited-scope investigator-initiated and sponsored studies, including management plans, indexes, meetings, completeness reviews, and issue escalation. The role also supports process improvements and computerized-system administration.

Manages early-phase clinical research projects from initiation through closure, coordinating sponsors, sites, CRAs, vendors, and internal teams. Oversees site activation, recruitment, monitoring deliverables, regulatory documentation, training, budgets, timelines, quality, risk, and change control. Supports clinical monitoring, TMF inspection readiness, data review, study trackers, and dashboards while ensuring compliance with GCP, ICH, FDA, Canadian regulations, SOPs, and study requirements.

Tracks and reports project profitability, budgets, revenues, expenses, forecasts, invoicing, and financial variances. Configures projects and budgets in financial systems, prepares journal entries and project reports, supports audits, advises project teams on cost control, and coordinates financial reviews with project managers and clients. The role also identifies process improvements and ensures accurate project financial records and account reconciliations.

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 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.

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.