Innovaderm Research

HQ
Montréal
Total Offices: 2
377 Total Employees
Year Founded: 2000

Jobs at Innovaderm Research

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Pharmaceutical • Manufacturing
Lead CRO business development for dermatology and rheumatology across Europe and the Middle East. Meet revenue targets, manage key accounts, negotiate contracts, develop sales strategies, represent the company at conferences, and collaborate with senior management to expand services and pricing strategies.
Pharmaceutical • Manufacturing
The Business Applications Analyst gathers business requirements, optimizes enterprise systems, and collaborates with stakeholders to ensure system needs are met efficiently.
Pharmaceutical • Manufacturing
Lead business development for the CRO unit across Europe and the Middle East: manage key accounts, meet sales targets, develop and execute sales strategies, support proposals and pricing, negotiate contracts, represent the company at scientific meetings, identify new services, and collaborate with senior management to drive revenue growth.
Pharmaceutical • Manufacturing
Lead CRO business development for dermatology and rheumatology across Europe and the Middle East. Manage key accounts, win new business, develop sales strategies, present proposals, negotiate contracts, represent the company at conferences, and drive revenue growth while collaborating with senior management and operations.
Pharmaceutical • Manufacturing
Lead CRO business development for dermatology and rheumatology across Europe and the Middle East. Meet revenue targets, manage key accounts, generate new business, represent the company at conferences, support proposals and pricing, negotiate contracts, and collaborate with senior management to develop growth strategies and new service offerings.
2 Days AgoSaved
In-Office or Remote
Montréal, QC, CAN
Pharmaceutical • Manufacturing
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.
Pharmaceutical • Manufacturing
The Administrative Assistant provides administrative support to the clinical research unit, manages office supplies, greets visitors, and assists in various administrative tasks.
2 Days AgoSaved
Remote
România
Pharmaceutical • Manufacturing
The Statistical Programmer develops and validates statistical datasets and programming for clinical trials, ensuring high-quality deliverables and compliance with industry standards.
2 Days AgoSaved
Remote
Argentina
Pharmaceutical • Manufacturing
The Project Manager oversees clinical research projects, ensuring compliance with budgets and timelines while coordinating various teams and stakeholders. Responsibilities include managing project deliverables, training team members, and maintaining stakeholder communication throughout the project lifecycle.
2 Days AgoSaved
Remote
Spain
Pharmaceutical • Manufacturing
The Project Manager oversees clinical research projects, ensuring compliance with budgets and timelines while coordinating tasks and team activities. Responsibilities include stakeholder communication, managing resources, training team members, and monitoring project quality and progress.
2 Days AgoSaved
Remote
România
Pharmaceutical • Manufacturing
The Project Manager oversees clinical research projects, ensuring compliance with budgets, timelines, and standards, while coordinating teams and stakeholders for project success.
Pharmaceutical • Manufacturing
The Senior Statistical Programmer leads clinical trials, develops specifications for datasets, validates programming, supports data cleaning, and collaborates on biostatistical deliverables.
2 Days AgoSaved
Remote
Canada
Pharmaceutical • Manufacturing
The Statistical Programmer develops, maintains, and validates datasets and reports for clinical trials, ensuring high-quality deliverables while adhering to industry standards and guidelines.
2 Days AgoSaved
Remote
Germany
Pharmaceutical • Manufacturing
The Project Manager oversees clinical research projects, ensuring compliance with budgets and timelines, coordinating tasks across departments, managing stakeholders, and supporting clinical monitoring activities.
2 Days AgoSaved
Remote
Poland
Pharmaceutical • Manufacturing
The Project Manager oversees clinical research projects, ensuring compliance with budgets, timelines, and regulatory standards while coordinating teams and stakeholders. Responsibilities include managing project tasks, monitoring patient recruitment, and maintaining project documentation and quality.
Pharmaceutical • Manufacturing
The Senior Statistical Programmer leads clinical trials, programming statistical data according to regulatory standards, and collaborates with teams to produce high-quality trial results.
2 Days AgoSaved
Remote
Argentina
Pharmaceutical • Manufacturing
The Statistical Programmer develops, maintains, and validates aCRFs, SDTM, ADaM datasets, and TLFs, ensuring compliance with guidelines and collaborating with teams for data quality and efficiency.
6 Days AgoSaved
In-Office or Remote
Montréal, QC, CAN
Pharmaceutical • Manufacturing
Design and produce high-quality visual assets across digital, print, presentation, and multimedia formats. Translate complex scientific and clinical content into clear, engaging visuals, develop templates and design systems, maintain brand consistency, create animations/videos/interactive content, and leverage AI tools to accelerate creative production while collaborating with stakeholders across marketing, communications, and business development.
12 Days AgoSaved
Remote
Argentina
Pharmaceutical • Manufacturing
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.
Pharmaceutical • Manufacturing
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.