Jobs at Innovaderm Research

Write, edit and maintain scientific and technical proposal content for CRO study bids. Coordinate SMEs and KOL input, manage RFI/RFP materials and templates, ensure compliance and quality, support proposal/contract managers and meet tight proposal timelines.

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.