
201 - 500 employees
đ Pharmaceuticals
đĽ Healthcare
đź Consulting
Pharmaceuticals ⢠Healthcare ⢠Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
đ Yesterday
Improve your chances of getting an interview by checking your resume score before you apply.

201 - 500 employees
đ Pharmaceuticals
đĽ Healthcare
đź Consulting
Pharmaceuticals ⢠Healthcare ⢠Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
⢠Serve as the main point of contact for site selection activities, including site identification and feasibility ⢠Develop and maintain relationships with key clinical research sites ⢠Identify investigators and research sites through literature and online searches ⢠Collect information to define ideal investigators for studies ⢠Identify and recommend potential investigators and sites ⢠Develop interest survey assessments ⢠Create and coordinate study-specific feasibility questionnaires ⢠Review feasibility questionnaires and recommend sites for qualification visits ⢠Coordinate CRA resource allocation for site qualification visits ⢠Review site qualification visit summaries ⢠Recommend sites for study participation in consultation with sponsors and project teams ⢠Track site selection activities in the Clinical Trial Management System (CTMS) ⢠Attend internal and external project team meetings as needed ⢠Identify site performance quality issues through project meetings, escalated communications, and quality assurance audit findings ⢠Participate in departmental projects related to site selection, contracting, and site intelligence ⢠Support the Manager, Site Selection in understanding project goals, scope, and requirements and delivering high-quality results
⢠Bachelorâs degree in science or relevant field of study ⢠Excellent oral and written skills in English; French is an asset ⢠Minimum of 3 years of experience in clinical research in the biotechnology, pharmaceutical, or CRO industry ⢠Significant and relevant experience in site selection, study start-up activities, site budget/contract negotiation, and/or working closely with sites or in a site environment ⢠Excellent knowledge of Microsoft Office suite (Word, Excel, PowerPoint) ⢠Experience in dermatological clinical research is an asset ⢠Good knowledge of good clinical practices and applicable Health Canada and FDA regulations/guidelines ⢠Ability to work in a team environment and establish good relationships with colleagues, sponsors, and sites ⢠Organized, able to juggle competing priorities, and work in a fast-paced, evolving environment ⢠Flexibility, positive attitude, superior attention to detail, and critical thinking skills ⢠Quick learner, good adaptability, and versatility ⢠Must be legally able to work in Poland
⢠Permanent full-time position ⢠Flexible schedule ⢠Vacation ⢠Home-based position ⢠Ongoing learning and development ⢠Attractive advancement opportunities ⢠Accommodation throughout the recruitment and selection process for applicants with disabilities, upon request
Apply Nowđ Yesterday
Senior Project Leader managing Workfront and Azure DevOps workflows for Avery Dennisonâs global materials science and digital identification business. Coordinating project delivery, Agile processes, reporting, and stakeholder alignment.
đ 3 days ago
Senior Site Specialist supporting investigator sites and clinical trial start-up for ICON, a global healthcare intelligence and research organisation. Home or office based in Warsaw or Sofia.
đŁď¸đłđą Dutch Required
đŁď¸đŤđˇ French Required
đ 4 days ago
Bottleneck specialist leading global supply-crisis response for MAHLEâs automotive manufacturing operations. Managing supplier escalations, material constraints, and executive recovery planning.
đ 4 days ago
Regional project lead delivering Seco SOLVAâs integrated manufacturing solutions. Coordinating customer projects, technical teams, partners, and measurable productivity improvements across East and Central Europe.
đ 4 days ago
Solva Regional Project Lead delivering end-to-end manufacturing improvement projects for Seco. Coordinating technical teams, partners, and customers across East and Central Europe.