Jobs at Innovaderm Research

Develop, maintain, and validate aCRFs, SDTM/ADaM datasets, define.XMLs, and TLFs using SAS and Pinnacle 21. Support data cleaning with Data Management, follow CDISC/ICH/regulatory standards, and improve programming efficiencies via macros and templates while collaborating with biostatistical teams.

Lead global clinical trial delivery for dermatology and/or rheumatology studies from start-up through closure. Serve as primary sponsor contact, manage budgets, timelines, vendors and cross-functional teams, ensure GCP/ICH compliance, prepare study deliverables, assess risk and quality, and drive recruitment and operational performance for multisite Phase III and other large multinational trials.

The Project Manager II is responsible for overseeing clinical trials, ensuring compliance with budgets and timelines, managing resources, leading teams, and communicating with stakeholders while maintaining quality standards.

The Project Manager II oversees clinical trials, ensuring compliance with budgets, timelines, and regulations while leading client interactions and project teams.

The Project Manager II is responsible for managing clinical trials, ensuring compliance with budgets, timelines, and regulations while serving as the primary communication link with stakeholders and overseeing resource coordination.

Lead multinational dermatology and/or rheumatology clinical trials from start-up to close. Act as sponsor contact, oversee study planning, budgets, timelines, quality, risk, vendor management, team leadership, and ensure audit readiness and recruitment targets across global regions.

Lead cross-functional teams to plan and execute multi-center Phase II-III clinical trials in dermatology (rheumatology a plus). Serve as sponsor contact, manage budgets and timelines (> $3M), ensure GCP/ICH/FDA compliance, maintain audit readiness, oversee vendors and site readiness, and report recruitment and study progress.

The Project Manager II oversees clinical trial operations, ensuring compliance with regulations, managing budgets and timelines, and leading project teams.

Lead global dermatology/rheumatology clinical trials from start-up to closure. Serve as sponsor primary contact, manage budgets, timelines, vendors, and cross‑functional teams, ensure GCP/ICH compliance, audit readiness, and recruitment tracking for multi‑center Phase III studies.

The Project Manager II oversees clinical trials, ensuring compliance with budgets, timelines, and regulatory standards. Key responsibilities include client interaction, project planning, quality management, budget control, and team leadership within the clinical research environment.

Lead multinational dermatology and/or rheumatology clinical trials from start-up through closure. Act as sponsor-facing primary contact, manage budgets, timelines, vendors, and cross-functional teams, ensure GCP/ICH compliance, audit readiness, and quality of study deliverables, and drive recruitment and risk mitigation for Phase III and large, multi-country studies.

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.

Lead end-to-end management of Phase I/II clinical trials including start-up, budgets, timelines, vendor and site management, risk mitigation, TMF oversight, regulatory compliance, and stakeholder communication.

Lead and coordinate early-phase clinical trials from start-up through close-out, managing budgets, timelines, vendors, TMF, monitoring, regulatory submissions, stakeholder communication, risk mitigation, training, and quality to ensure GCP and regulatory compliance.

Lead planning, execution, monitoring, and closure of early-phase (Phase I/II) clinical trials. Manage budgets, timelines, vendors, TMF, site activation, regulatory submissions, quality control, risk mitigation, stakeholder communication, and cross-functional coordination. Support monitoring activities, CRA training, recruitment tracking, and may mentor junior staff or contribute to business development and process improvements.

Lead end-to-end operational management of Phase I/II clinical trials: oversee timelines, budgets, vendors, TMF, site activation, monitoring oversight, risk mitigation, stakeholder communication, and regulatory compliance. Support feasibility, study start-up, training, quality control, and cross-functional coordination; mentor junior staff and contribute to process improvement and business development.

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

Lead and oversee a portfolio of global clinical studies in dermatology and rheumatology, managing Project Managers, budgets, timelines, regulatory compliance (GCP/ICH/FDA), vendor relationships, risk mitigation, and client communications. Provide operational input to proposals, drive performance improvements, and mentor project management staff to ensure successful study delivery.

Lead oversight of a portfolio of dermatology and rheumatology clinical trials, managing Project Managers, ensuring GCP/ICH compliance, budgets, timelines, vendor management, risk mitigation, proposal input, and client relations for global, multi-center programs.

Lead oversight of a portfolio of clinical studies in dermatology or rheumatology, manage Project Managers, ensure regulatory compliance (GCP, FDA), drive budgeting, risk mitigation, proposal input, vendor management, and client satisfaction across multinational Phase III and large trials.